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Accu-Chek Fastclix

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Operations, Inc.

Identity

Trade Name
Accu-Chek Fastclix FDA UDI
Generic Name
Manual blood lancing device, reusable FDA UDI
Device Name
Accu-Chek Fastclix Kit Canada FDA UDI
Model / Reference
09917756001 FDA UDI
Description
Accu-Chek Fastclix Kit Canada FDA UDI

Identifiers

Catalog Number
09917756001 FDA UDI
Primary DI / UDI-DI
00365702702806 FDA UDI
FDA Product Code
QRL FDA UDI
GMDN Term
Manual blood lancing device, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

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

Yes

FDA UDI

Category: Blood lancing device tipManual blood lancing device, reusable

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

Similar devices

Also classified as Manual blood lancing device, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6b72fb30-514c-4d2b-aedb-47fad59190d6 34 fields · synced May 30, 2026