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Hammr™ 110049103

by Biomet Orthopedics, Inc.

Hammr™ 110049103 is a Class I device made by Biomet Orthopedics, Inc., listed in FDA GUDID since 9 May 2024 (UDI-DI 00889024663824), 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 Number00889024663824 UDI-DI Date9 May 2024ListedStatusListed 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  • Withdrawn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
Hammr™
Generic name
Surgical power tool adaptor
Model / Ref / Catalog
110049103
Primary DI / UDI-DI
00889024663824
FDA product code
GEY
GMDN term
Surgical power tool adaptor
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical power tool adaptor

Similar devices in this category

Other devices filed under Surgical power tool adaptor.

Other devices from Biomet Orthopedics, Inc.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)