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A1CNow®+ Multi-Use Test System (10 count)

FDA UDI

Class II (US FDA UDI)

by Polymer Technology Systems

Identity

Trade Name
A1CNow®+ Multi-Use Test System (10 count) FDA UDI
Generic Name
Glycated haemoglobin (HbA1c) monitoring system IVD, point-of-care FDA UDI
Device Name
The A1CNow®+ Multi-Use Test System provides quantitative measurement of the percent of glycated hemoglobin (%HbA1C or %A1C) levels in human whole blood samples. FDA UDI
Model / Reference
3024 FDA UDI
Description
The A1CNow®+ Multi-Use Test System provides quantitative measurement of the percent of glycated hemoglobin (%HbA1C or %A1C) levels in human whole blood samples. FDA UDI

Identifiers

Catalog Number
3024 FDA UDI
Primary DI / UDI-DI
00381933024012 FDA UDI
510(k) Number
K090413 FDA UDI
FDA Product Code
LCP FDA UDI
GMDN Term
Glycated haemoglobin (HbA1c) monitoring system IVD, point-of-care FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.7470 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

No

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: Glycated haemoglobin (HbA1c) monitoring system IVD, point-of-care

A1CNow®+ Multi-Use Test System (10 count) by Polymer Technology Systems — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glycated haemoglobin (HbA1c) monitoring system IVD, point-of-care.

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 6b211703-5905-42a3-970f-62d3d0e4aa9a 37 fields · synced May 30, 2026