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Air Filter AF-D1

by Bmc Medical., Ltd.

Air Filter AF-D1 is a Class II device made by Bmc Medical., Ltd., listed in FDA GUDID since 22 Sep 2022 (UDI-DI 06948538362853), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06948538362853 UDI-DI Date22 Sep 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  • Withdrawn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
Air Filter
Generic name
Home BPAP unit
Model / reference
AF-D1
Primary DI / UDI-DI
06948538362853
FDA product code
BZD
GMDN term
Home BPAP unit
Device class
Class II
Regulation number
868.5905
GUDID distribution status
In Commercial Distribution

Related devices

Category: Home BPAP unit

Similar devices

Other devices filed under FDA product code BZD (Ventilator, Non-Continuous (Respirator)).

Other devices from Bmc Medical., Ltd.

See all devices from Bmc Medical., Ltd. →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)