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Relion 09556672001

by Roche Diagnostics Operations, Inc.

Relion 09556672001 is a Class II device made by Roche Diagnostics Operations, Inc., listed in FDA GUDID since 19 Oct 2022 (UDI-DI 00365702702660), 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 Number00365702702660 UDI-DI Date19 Oct 2022ListedStatusListed 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  • Withdrawn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
Relion
Generic name
Manual blood lancing device, reusable
Model / Ref / Catalog
09556672001
Primary DI / UDI-DI
00365702702660
FDA product code
QRL
GMDN term
Manual blood lancing device, reusable
Device class
Class II
Regulation number
878.4850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood lancing device tipManual blood lancing device, reusable

Similar devices

Other devices filed under FDA product code QRL (Multiple Use Blood Lancet For Single Patient Use Only).

Other devices from Roche Diagnostics Operations, Inc.

See all devices from Roche Diagnostics Operations, Inc. →

Properties

  • Lot / batch number
Other properties (14, all answered No)