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CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ (2-pk)

FDA UDI

Class II (US FDA UDI)

by Polymer Technology Systems

Identity

Trade Name
CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ (2-pk) FDA UDI
Generic Name
Multiple clinical chemistry enzyme IVD, kit, spectrophotometry FDA UDI
Device Name
CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ are in vitro diagnostic devices used to monitor glucose and lipid (total cholesterol / HDL cholesterol / and triglyceride) levels in human whole blood. These test strips must be used in conjunction with a CardioChek Plus analyzer. FDA UDI
Model / Reference
2729 FDA UDI
Description
CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ are in vitro diagnostic devices used to monitor glucose and lipid (total cholesterol / HDL cholesterol / and triglyceride) levels in human whole blood. These test strips must be used in conjunction with a CardioChek Plus analyzer. FDA UDI

Identifiers

Catalog Number
2729 FDA UDI
Primary DI / UDI-DI
00381932729017 FDA UDI
510(k) Number
K022898 FDA UDI
K023558 FDA UDI
K140068 FDA UDI
FDA Product Code
CGA FDA UDI
JGY FDA UDI
LBR FDA UDI
CHH FDA UDI
NBW FDA UDI
GMDN Term
Multiple clinical chemistry enzyme IVD, kit, spectrophotometry FDA UDI

Classification

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

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple lipid analyte IVD, kit, multiple technologiesMultiple clinical chemistry enzyme IVD, kit, spectrophotometry

CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ (2-pk) by Polymer Technology Systems — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Multiple clinical chemistry enzyme IVD, kit, spectrophotometry.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fdcb6735-9a33-4208-8714-6783156507d0 37 fields · synced May 31, 2026