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02-5402

by Biomet Microfixation, Inc

02-5402 is a Class I device made by Biomet Microfixation, Inc, listed in FDA GUDID since 16 Jun 2017 (UDI-DI 00841036022082), 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 Number00841036022082 UDI-DI Date16 Jun 2017ListedStatusListed 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  • Withdrawn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

Generic name
Manual bone mill
Model / Ref / Catalog
02-5402
Primary DI / UDI-DI
00841036022082
FDA product code
LYS
GMDN term
Manual bone mill
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Manual bone mill

Similar devices in this category

Other devices filed under Manual bone mill.

Other devices from Biomet Microfixation, Inc

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Properties

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