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Compass AW-.050-10

by Compass International

Compass AW-.050-10 is a Class II device made by Compass International, listed in FDA GUDID since 8 Jul 2016 (UDI-DI B169AW050100), 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 NumberB169AW050100 UDI-DI Date8 Jul 2016ListedStatusListed GUDID: 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  • Withdrawn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
Compass
Generic name
Surgical screwdriver, reusable
Model / Ref / Catalog
AW-.050-10
Primary DI / UDI-DI
B169AW050100
FDA product code
HAW
GMDN term
Surgical screwdriver, reusable
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution

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Properties

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