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Accu-Chek Fastclix

FDA UDI

Class II (US FDA UDI)

by Roche Diabetes Care, Inc.

Identity

Trade Name
Accu-Chek Fastclix FDA UDI
Generic Name
Manual blood lancing device, reusable FDA UDI
Device Name
Accu-Chek Fastclix Device Bulk 100 FDA UDI
Model / Reference
07523211001 FDA UDI
Description
Accu-Chek Fastclix Device Bulk 100 FDA UDI

Identifiers

Catalog Number
07523211001 FDA UDI
Primary DI / UDI-DI
04015630065615 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood lancing device tipManual blood lancing device, reusable

Accu-Chek Fastclix by Roche Diabetes Care, 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 af3b8934-093e-4a92-b7ee-cd903a490fa5 34 fields · synced May 30, 2026