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Accu-Chek Performa 07299702001

by Roche Diagnostics Operations, Inc.

Accu-Chek Performa 07299702001 is a Class II device made by Roche Diagnostics Operations, Inc., listed in FDA GUDID since 26 Aug 2016 (UDI-DI 00365702602106), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00365702602106 UDI-DI Date26 Aug 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Accu-Chek Performa
Generic name
Glucose IVD, reagent
Model / Ref / Catalog
07299702001
Primary DI / UDI-DI
00365702602106
FDA product code
LFR
GMDN term
Glucose IVD, reagent
Device class
Class II
Regulation number
862.1345
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LFR (Glucose Dehydrogenase, Glucose).

Other devices from Roche Diagnostics Operations, Inc.

See all devices from Roche Diagnostics Operations, Inc. →

Properties

  • Lot / batch number
  • Expiration date
Other properties (13, all answered No)