Accu-Chek Guide

FDA UDI

Class I (US FDA UDI)

by Roche Diagnostics Operations, Inc.

Identity

Trade Name: ACCU-CHEK GUIDE FDA UDI
Generic Name: Glucose IVD, control FDA UDI
Device Name: ACCU-CHEK GUIDE 2-LEVEL CONTROLS US FDA UDI
Model / Reference: 07748906001 FDA UDI
Description: ACCU-CHEK GUIDE 2-LEVEL CONTROLS US FDA UDI

Identifiers

Primary DI / UDI-DI: 00365702688100 FDA UDI
FDA Product Code: JJX FDA UDI
GMDN Term: Glucose IVD, control FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 862.1660 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Glucose IVD, control

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Roche Diagnostics Operations, Inc.

Sources (1)

FDA UDI 81115b25-695b-4c58-bcde-17f823ec4ee1 33 fields · synced Jun 1, 2026