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Accu-Chek Guide

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Operations, Inc.

Identity

Trade Name
Accu-Chek Guide FDA UDI
Generic Name
Glucose analyser IVD, home-use FDA UDI
Device Name
ACCU-CHEK GUIDE MG/DL METER 923 (US) FDA UDI
Model / Reference
07398794001 FDA UDI
Description
ACCU-CHEK GUIDE MG/DL METER 923 (US) FDA UDI

Identifiers

Primary DI / UDI-DI
00365702609105 FDA UDI
510(k) Number
K160944 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Glucose analyser IVD, home-use 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose analyser IVD, home-use

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

Similar devices

Also classified as Glucose analyser IVD, home-use.

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 8652adf3-2a0e-4467-add4-5706a74318e6 34 fields · synced Jun 8, 2026