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Bose Frames BMD0005

by Bose Corporation 3 variants

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00017817812818 UDI-DI Date8 Jul 2021ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Bose Frames
Generic Name
Tinted non-prescription spectacle lens
Model / Ref / Catalog
BMD0005, 833416-010R
Primary DI / UDI-DI
00017817812818
FDA Product Code
HQY, HQZ
GMDN Term
Tinted non-prescription spectacle lens
Device Class
Class I
Regulation Number
886.5850, 886.5842
GUDID distribution status
Not in Commercial Distribution

Other devices from Bose Corporation

Properties

  • Prescription Use
  • Over-the-Counter
  • Premarket Exempt

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No