Sugentech, Inc. of Cheongju-si, Chungcheongbuk-do at MEDICA 2017 in Düsseldorf -- MEDICA Trade Fair
Premium Exhibitor Manufacturers OEM

Sugentech, Inc.

721-26 Jeongjungyeonje-ro, Osong-eup, Heungdeok-gu, 28161 Cheongju-si, Chungcheongbuk-do
Korea, Republic

Telephone +82 2 22265282
Fax +82 43 7102880
info@sugentech.com

Hall map

MEDICA 2017 hall map (Hall 3A): stand 3AD55

Fairground map

MEDICA 2017 fairground map: Hall 3A

Contact

LUCIO KIM

General Manager (POCT business)
Overseas Sales & Marketing

Korea, Republic

Phone
0082222265005

Email
luciokim@sugentech.com

JIYOUNG KWAK

Senior Sales Manager(OTC business)
Overseas Sales & Marketing

Korea, Republic

Phone
0082222265282

Email
jyoung@sugentech.com

Heonju Lee

Sales manager (instrument OEM&ODM)
Overseas Sales & Marketing

Korea, Republic

Phone
+82-43-710-2806

Email
leehj@sugentech.com

Our range of products

Product categories

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.01  Allergies

Allergies

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.03  Auto-immune diseases

Auto-immune diseases

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.04  Fertility / Pregnancy hormones / Proteins

Fertility / Pregnancy hormones / Proteins

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.05  Units and systems for hormone determination
  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.06  Thyroid function hormones

Thyroid function hormones

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.06  Thyroid function hormones
  • 03.02.06.01  Diagnostic agents / kits for thyroid gland, etc. determination (Thyroid function hormones)

Diagnostic agents / kits for thyroid gland, etc. determination (Thyroid function hormones)

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.06  Thyroid function hormones
  • 03.02.06.02  Units and systems for the determination of thyroid glands hormones

Units and systems for the determination of thyroid glands hormones

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.07  Immuno assay systems
  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.07  Immuno assay systems
  • 03.02.07.09  Fluorometric assay

Fluorometric assay

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.07  Immuno assay systems
  • 03.02.07.13  Immunoblots / dotblots
  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.07  Immuno assay systems
  • 03.02.07.19  Photometric assay
  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.07  Immuno assay systems
  • 03.02.07.25  Time-delayed fluorescence immunoassay (TRFIA)

Time-delayed fluorescence immunoassay (TRFIA)

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.07  Immuno assay systems
  • 03.02.07.27  Time-delayed immunofluorometric assay (TRIFMA)

Time-delayed immunofluorometric assay (TRIFMA)

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.14  Specific proteins

Specific proteins

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.14  Specific proteins
  • 03.02.14.01  C-reactive proteins (CRP)
  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.15  Rapid tests - Immunochemistry
  • 03.02.15.01  Pregnancy tests
  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.15  Rapid tests - Immunochemistry
  • 03.02.15.02  Infectious disease tests
  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.16  Therapeutic drug monitoring

Therapeutic drug monitoring

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.16  Therapeutic drug monitoring
  • 03.02.16.01  Diagnostic agents / kits for determination of therapeutic drugs

Diagnostic agents / kits for determination of therapeutic drugs

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.16  Therapeutic drug monitoring
  • 03.02.16.02  Units and systems for the determination of therapeutic drugs

Units and systems for the determination of therapeutic drugs

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.17  Tumor markers

Tumor markers

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.17  Tumor markers
  • 03.02.17.01  Diagnostic agents / kits for tumour marker determination

Diagnostic agents / kits for tumour marker determination

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.17  Tumor markers
  • 03.02.17.02  Units and systems for tumour marker determination

Units and systems for tumour marker determination

  • 03  Diagnostics
  • 03.02  Immunochemistry (Immunology)
  • 03.02.18  Sepsis markers

Our products

Product category: Immuno assay systems, Photometric assay

INCLIX, Quantitative Immunoassay Analyzer (CE marked)

INCLIX™ is an immunochromatographic analyzer providing immediate point-of-care testing (POCT) at patient care settings or clinical laboratories. It facilitates automatic detection of various biomarkers for cardiovascular disease, infectious disease, cancer, diabetes, allergy, and etc. with high accuracy and sensitivity.

INCLIX™ analyzer is a compact, easy-to-use and cost-effective multi-parameter POCT instrument  and its unique user friendly software provides an efficient data management system. 

* Parameters Available with CE mark: HbA1c, PCT, Troponin I, CRP, hsCRP, Dual CRP(CRP+hs-CRP), Influenza A&B
* Other tests (β-hCG, Total-hCG, Total IgE, PSA, TSH, T3, T4, Vitamin D, D-dimer, Zika IgM/IgG, etc.) are also coming soon in 2018.

• Good accuracy owning to superior CMOS sensor & our own Algorism
• 10,000 test results data storage 
• Instrument Check by Reference Kit
• Remote Support available (when connected via Internet)
• Built-in Thermal Printer and Barcode Scanner
• Data export to USB(PDF, Excel), Email and LIS
• Storage Temperature of Test Cassette & Buffer : Room temperature, 2 ~ 30 ℃
• Shelf Life of Test Cassette & Buffer : 24 months

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Product category: Rapid tests - Immunochemistry

INCLIX HbA1c Test (CE marked, NGSP certified)

INTENDED USE
INCLIX™ HbA1c along with INCLIX™ Analyzer is an immunochromatographic in-vitro diagnostic device for quantitative determination of Glycated Hemoglobin (HbA1c) in human blood. The test is used as an aid to diagnose diabetes and for monitoring long-term glycemic control in patients with diabetes.

PRINCIPLE
This test uses a sandwich immunoassay using gold nanoparticle-based immunochromatographic method. When dropping the specimen diluted in diluent buffer to the sample well of the cassette, it moves through the nitrocellulose membrane on the strip.
The antigen-antibody complex is combined with the capture antibody and it is colored as purple red by gold particle.
The intensity of the band depends on quantity of glycated hemoglobin molecules.
Results are automatically calculated by INCLIX™ Analyzer and the HbA1c concentration can be verified immediately.

Specifications
• Sample Type : Whole blood
• Sample Volume : Whole blood 5μL
• Measuring range : 4-14%
• Precision : <10% CV in working range.
• Measuring time : 3 minutes
• Storage temperature: 2-30°C (36-86°F)
• Shelf Life : 24 months

Method comparison
Comparison studies between the candidate device (INCLIX™ HbA1c) and the predicate device (Tosoh, HLC-723 G11) were conducted by lab professionals, using 100 specimens. The linear regression line and correlation coefficient were found to be : y = 1.002x + 0.0135; R = 0.9875.

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Product category: Rapid tests - Immunochemistry, Sepsis markers

INCLIX PCT Test (CE marked)

INTENDED USE
INCLIX™ PCT along with INCLIX™ Analyzer is an immunoassay for quantitative determination of Procalcitonin (PCT) in human serum/plasma. The test is useful in the diagnosis of bacterial infection and sepsis.

PRINCIPLE
This test uses a sandwich immunoassay using gold nanoparticle-based immunochromatographic method. When dropping the specimen diluted in diluent buffer to the sample well of the cassette, it moves through the nitrocellulose membrane on the strip.
The antigen-antibody complex is combined with the capture antibody and it is colored as purple red by gold particle.
The intensity of the band depends on quantity of PCT molecules. Results are automatically calculated by INCLIX™ analyzer and the PCT concentration can be verified immediately.

Specifications
• Sample Type : Serum or Plasma
• Sample Volume : 100uL
• Measuring range : 0.25- 40 ng/mL (Cutoff 0.5 ng/mL)
• Precision : <15% CV in working range
• Measuring time : 15 minutes
• Storage temperature: 2-30°C (36-86°F)
• Shelf Life : 24 months

Method comparison
Comparison studies between the candidate device (INCLIX™ PCT) and the predicate device (ADVIA Centaur™ XP PCT) were conducted by lab professionals, using 123 specimens. The linear regression line and correlation coefficient were found to be : y=1.074x + 0.080; R =0.979

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Product category: Rapid tests - Immunochemistry

INCLIX Troponin I (CE marked)

INTENDED USE
diagnostic device for quantitative determination of cardiac Troponin I (TnI) in serum, plasma and whole blood. The test is used as an aid to diagnose Acute Myocardial Infarction
(AMI).

PRINCIPLE
This test uses a sandwich immunoassay using gold nanoparticle-based immunochromatographic method. When dropping the specimen diluted in diluent buffer to the sample well of the cassette, it moves through the nitrocellulose membrane on the strip.
The antigen-antibody complex is combined with the capture antibody and it is colored as purple red by gold particle.
The intensity of the band depends on quantity of Troponin I molecules. Results are automatically calculated by INCLIX™ Analyzer and the Troponin I concentration can be verified immediately. Troponin I concentrations are expressed as ng/mL.

Specifications
• Sample Type : Whole blood, serum, or plasma
• Sample Volume : 100uL
• Measuring range : 0.1 - 50 ng/mL
• Precision : <10% CV in working range
• Measuring time : 10 minutes
• Storage temperature: 2-30°C (36-86°F)
• Shelf Life : 24 months

Method comparison
Comparison studies between the candidate device (INCLIX™ Troponin I) and the predicate device (i-CHROMA™ Tn-I) were conducted by lab professionals, using 105 specimens. The linear regression line and correlation coefficient were found to be : y =
0.955x + 1.823; R = 0.9593.

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Product category: C-reactive proteins (CRP)

INCLIX CRP / hsCRP / dual CRP Test (CE marked)

PRINCIPLE
This test uses a sandwich immunoassay using gold nanoparticle-based immunochromatographic method. When dropping the specimen diluted in diluent buffer to the sample well of the cassette, it moves through the nitrocellulose membrane on the strip.
The antigen-antibody complex is combined with the capture antibody and it is colored as purple red by gold particle.
The intensity of the band depends on quantity of CRP molecules. Results are automatically calculated by INCLIX™
analyzer and the CRP concentration can be verified immediately.

Specifications
• Sample Type : Whole blood, serum, or plasma
• Sample Volume : 5uL
• Measuring range (CRP) : 2.5 - 300 mg/L (Cutoff 10 mg/L)
• Measuring range (hsCRP) : 0.1 – 10 mg/L (Cutoff 1 mg/L)
• Measuring range (dual CRP) : 0.5 – 200 mg/L (Inflammation cutoff 10mg/L, cardiovascular disease cutoff 1 mg/L)
• Precision : <10% CV in working range
• Measuring time : 5 minutes
• Storage Temperature : 2-30°C (36-86°F)
• Shelf Life : 24 months

Method comparison (CRP)
Comparison studies between the candidate device (INCLIX™ CRP) and the predicate device (ADVIA 1800 CRP) were conducted by lab professionals, using 200 specimens. The linear regression line and correlation coefficient were found to be : y = 0.903x + 1.216; R = 0.991

Method comparison (hsCRP)
Comparison studies between the candidate device (INCLIX™ hsCRP) and the predicate device (ADVIA 1800 CRP, Wide range) were conducted by lab professionals, using 200 specimens. The linear regression line and correlation coefficient were found to be : y =
1.080x – 0.219; R = 0.981.

Method comparison (dual CRP)
Comparison studies between the candidate device (INCLIX™ dual CRP) and the predicate device (ADVIA 1800 CRP, Wide range) were conducted by lab professionals, using 200 specimens. The linear regression line and correlation coefficient were found
to be : y = 1.118x - 0.728; R = 0.994.

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Product category: Rapid tests - Immunochemistry, Infectious disease tests

SGT i-flex Influenza A&B Test (CE marked, qualitative assay)

INTENDED USE
SGT i-flex Influenza A&B is an immunoassay for qualitative detection of Influenza virus type A or type B antigens directly from nasopharyngeal swab specimens. The test is used as an aid to detect the influenza viruses by simultaneously distinguishing between A and B, which are human-infected subtypes. The test is not intended to detect influenza C antigens. 

PRINCIPLE
The principle of SGT Influenza A & B is the qualitative assay to detect influenza virus in the nasopharynx. Influenza virus swabs from nasopharynx are suspended in sample extracts and the suspension is dispensed into the kit. Influenza virus nucleoprotein allows the diagnosis of influenza viruses through visual inspection and analytical device by antigen-antibody immunochromatography combined with nucleoprotein specific antibody and gold in the kit. It is also possible to diagnose influenza A and B simultaneously and separately.

Specifications
• Sample Type : nasopharyngeal swab
• Sample extraction time : 5 minutes
• Extracted sample loading volume: 4 drops
• Reaction time: 10 minutes after loading the sample
• Storage temperature: 2-30°C (36-86°F)
• Shelf Life : 24 months

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Product category: Units and systems for hormone determination, Pregnancy tests

Surearly Digital Pregnancy Test (US FDA & CE certified)

Korea’s First & No.1 Digital Test
ACCURATE and SIMPLE!
Test result is displayed on LCD with digital word (YES or NO) and symbol.

• Single-use or multiple-use type
• Rapid, Easy-to -Read DIGITAL results in about 3 minutes
• Over 99% accurate
• User’s procedural error detection
• hCG hormone detection in urine
• Sensitivity level of 25mIU/mL

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Product category: Fertility / Pregnancy hormones / Proteins, Units and systems for hormone determination, Rapid tests - Immunochemistry

Surearly Digital Ovulation Test (US FDA, CE marked)

Korea’s First & No.1 Digital Ovulation Test
EASY-TO-READ and ACCURATE!
Test result is displayed on LCD with digital word and symbol.
[YES means ovulation will soon occur within the next 24~36 hours.]

• Rapid, Easy-to -Read DIGITAL results in 3 minutes
• Over 99% accurate
• User’s procedural error detection
• LH hormone detection in urine
• Sensitivity level of 25mIU/mL

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Product category: Immunoblots / dotblots

Immunoblot strip assay analyzer(CE marked)

Sugentech’s Automatic systems of immunoblot and western blot guarantee much faster and more accurate result of measurement, it is designed to be more convenient, stable and user friendly with over 10 years experience.

This automatic system makes all the diagnosis process like Western Blot and Hybridization Strips automatically and it can be customized on your various applications and requirements.

User-friendly customizing software and rapid customer service of device and the one for the most outstanding advantages only provided by Sugentech

K-Blot Supreme
Full automation system
●  Sample Identification - Sample - Incubation- Drying – Analysis - Auto Cleaning
● Up to 40 samples analysis per run
●  hLLD (pressure & capacitive liquid level detection)
●  Real Time Pump Calibration → Reliable Dispensing accuracy
● Smart moving camera
 
K-Blot 48
Semi automation system
● Sample(Manual) – Incubation – Drying - Analysis- Auto Cleaning
● Up to 48 samples analysis per run
● Detect concentration of specific antibody by membrane
● High accurate dispensing module
● Sensitive and stable result by high resolution detector
 
K-Blot Lite
Liquid handler
● Incubation - Dry - Auto Cleaning
● Up to 20 samples per run
● Efficient Drying Module → Rapidly obtain result
● High dispensing Accuracy
● Compact Design

K-Screen
Strip Reader
● Rapid quantities immunoassay analyzer
    Color & Fluorescence & TRF 
● Multiple test
● Sensitive and stable results by high resolution detector
● 7 inch Touch Screen
● Useful data treatment

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About us

Company details

Sugentech is the 28th INNOPOLIS Research Institute Spin-off Company of Ministry of Science, ICT and Future Planning, Korea, which was established in 2011 by experienced executives and technical experts in the field of in-vitro diagnostics. 

We are an US FDA registered and ISO13485 certified in-vitro diagnostics company, providing next-generation personal point -of -care testing(POCT) products based on BT, IT, and NT.
As an innovative diagnostics company, Sugentech provides reliable and excellent information through rapid diagnostic tests with the leading-edge technology you need.

Sugentech recently completed the acquisition of the K-MAC BioCenter, a subsidary of K-MAC (Korea Materials & Analysis corp). K-MAC BioCenter is specialized in providing high technnology of instrument optimization of in-vitro diagnostics.
This is a significant milestone in our long-term strategy to move forward to become a global leading IVD manufacturer.
 This will be the first major step in that journey and we will take a quantum leap toward securing our competitive position in that space.

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Company data

Sales volume

50-99 Mio US $

Export content

max. 50%

Number of employees

50-99

Foundation

2011

Area of business
  • Laboratory Equipment
  • Diagnostics

Company information as a PDF file