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OsteoMed 220-0310

by Osteomed Corp.

Part of a family of 80 devices: see the family page

Ref 220-0310Model DRILL

OsteoMed 220-0310 is a device classified as Class IIa and Class IIb in the EU and Class II in the US made by Osteomed Corp., registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI 0806378BUDIO55S5) and listed in FDA GUDID since 22 Sep 2017 (UDI-DI 00845694015042), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDR CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number0806378BUDIO55S5 Basic UDI-DI 00845694015042UDI-DIDate5 Oct 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number0806378BUDIO55S5 Basic UDI-DI 00845694015042UDI-DIDate5 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00845694015042 UDI-DI Date22 Sep 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0806378BUDIO55S5 registered 5 Oct 2026 Active· +1 more in the status table
  • FDA GUDID UDI-DI 00845694015042 listed 22 Sep 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00845694015042
  2. Registered EUDAMED 0806378BUDIO55S5

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD, CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Acumed EUDAMED
OsteoMed GUDID
Generic name
General internal orthopaedic fixation system implantation kit
Device name
Drill
Model / Ref / Catalog
220-0310, DRILL
Primary DI / UDI-DI
00845694015042
Basic UDI-DI
0806378BUDIO55S5, B-00845694015042
FDA product code
KMW
EMDN code
P091303, L091002
GMDN term
General internal orthopaedic fixation system implantation kit
Device class
Class IIa EUDAMED
Class IIb EUDAMED
Class II GUDID
Regulation number
872.4120
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 4.5 Inch

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa and Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes.

Related devices

Category: General internal orthopaedic fixation system implantation kit

Similar devices in this category

Other devices filed under INSTRUMENTS FOR PROCESSING MATERIALS FOR OSTEOSYNTHESIS, REUSABLE.

Other devices from Osteomed Corp.

See all devices from Osteomed Corp. →

Properties

  • Sterilise before use
  • Single use
  • Reusable
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)