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CardioChek® Plus Professional Analyzer

FDA UDI

Class I (US FDA UDI)

by Polymer Technology Systems

Identity

Trade Name
CardioChek® Plus Professional Analyzer FDA UDI
Generic Name
Multiple clinical chemistry analyser IVD, point-of-care FDA UDI
Device Name
The CardioChek® Plus professional analyzer is intended for in vitro diagnostic use to test whole blood. The specific analyte measured is determined by the type of test strip chosen. FDA UDI
Model / Reference
2700 FDA UDI
Description
The CardioChek® Plus professional analyzer is intended for in vitro diagnostic use to test whole blood. The specific analyte measured is determined by the type of test strip chosen. FDA UDI

Identifiers

Catalog Number
2700 FDA UDI
Primary DI / UDI-DI
00381932700016 FDA UDI
FDA Product Code
LBR FDA UDI
CHH FDA UDI
CGA FDA UDI
NBW FDA UDI
JGY FDA UDI
GMDN Term
Multiple clinical chemistry analyser IVD, point-of-care FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1475 FDA UDI
862.1175 FDA UDI
862.1345 FDA UDI
862.1705 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multiple clinical chemistry analyser IVD, point-of-care

CardioChek® Plus Professional Analyzer by Polymer Technology Systems — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple clinical chemistry analyser IVD, point-of-care.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b90ea9c6-0a79-4ff7-ae2b-2fa94ef95bda 36 fields · synced Jun 1, 2026