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Bone cutters 108116

by DFS - DIAMON GmbH

Bone cutters 108116 is a Class I device made by DFS - DIAMON GmbH, listed in FDA GUDID since 30 Nov 2020 (UDI-DI 04057176148865), 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 Number04057176148865 UDI-DI Date30 Nov 2020ListedStatusListed 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  • Withdrawn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
Bone cutters
Generic name
Steel dental bur, reusable
Model / reference
108116
Primary DI / UDI-DI
04057176148865
FDA product code
EJL
GMDN term
Steel dental bur, reusable
Device class
Class I
Regulation number
872.3240
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Properties

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