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Accu-Check Guide

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Operations, Inc.

Identity

Trade Name
ACCU-CHECK GUIDE FDA UDI
Generic Name
Glucose IVD, reagent FDA UDI
Device Name
ACCU-CHEK GUIDE CASH US 60CT STRIP FDA UDI
Model / Reference
10439238001 FDA UDI
Description
ACCU-CHEK GUIDE CASH US 60CT STRIP FDA UDI

Identifiers

Catalog Number
10439238001 FDA UDI
Primary DI / UDI-DI
00365702703254 FDA UDI
510(k) Number
K160944 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Glucose IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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

No

FDA UDI

Over-the-Counter

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose IVD, reagent

Accu-Check Guide by Roche Diagnostics Operations, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose IVD, reagent.

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 5c199778-f4de-4253-999a-1d8d6d8553a4 35 fields · synced May 29, 2026