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Bosma Enterprises 10-8020PAO

by Bosma Enterprises

Bosma Enterprises 10-8020PAO is a Class I device made by Bosma Enterprises, listed in FDA GUDID since 14 May 2026 (UDI-DI 00818634020635), 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 Number00818634020635 UDI-DI Date14 May 2026ListedStatusListed 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  • Withdrawn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
Bosma Enterprises
Generic name
Operating room turnover kit
Model / Ref / Catalog
10-8020PAO
Primary DI / UDI-DI
00818634020635
FDA product code
PWU
GMDN term
Operating room turnover kit
Device class
Class I
Regulation number
880.6890
GUDID distribution status
In Commercial Distribution

Other devices from Bosma Enterprises

See all devices from Bosma Enterprises →

Properties

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