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Bbig TR22045386

by BBig B.V.

Bbig TR22045386 is a Class I device made by BBig B.V., listed in FDA GUDID since 15 Oct 2017 (UDI-DI 08719616045160), 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 Number08719616045160 UDI-DI Date15 Oct 2017ListedStatusListed 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  • Withdrawn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
Bbig
Generic name
Spectacle frame
Model / reference
TR22045386
Primary DI / UDI-DI
08719616045160
FDA product code
HQZ
GMDN term
Spectacle frame
Device class
Class I
Regulation number
886.5842
GUDID distribution status
In Commercial Distribution

Related devices

Category: Spectacle frame

Other devices from BBig B.V.

See all devices from BBig B.V. →

Properties

  • Single use
  • Premarket exempt
Other properties (13, all answered No)