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Restore Bayonet Point Pin with Eyelet

by Medos International SARL 3 variants

Ref 219322Model General Surgical Instruments

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

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0886705a00096KW Basic UDI-DI 10886705005734UDI-DIDate30 Dec 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10886705005734 UDI-DI Date1 Sep 2015ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Restore Bayonet Point Pin with Eyelet EUDAMED
Restore GUDID
Generic Name
Orthopaedic bone pin, non-bioabsorbable
Device Name
Guide Pin, Trocar Point, Drill Point, Bay Pin, Eyelet, Drill Pin, Passing Pin, Trocar Tip, Drill Trip, Calibrated
Model / Ref / Catalog
General Surgical Instruments, 219322
Primary DI / UDI-DI
10886705005734
Basic UDI-DI
0886705a00096KW
Direct Marketing DI
10886705005734
FDA Product Code
NBH
EMDN Code
L0999 Orthopaedic and traumatological surgery instruments, reusable - other
GMDN Term
Orthopaedic bone pin, non-bioabsorbable
Device Class
Class IIa EUDAMED
Class I GUDID
Regulation Number
888.1100
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class I
ImplantableEUDAMED
No
GUDID
Yes

Manufacturer details

EUDAMED SRN
CH-MF-000014268
Authorised representative
DePuy Ireland UC IE-AR-000009328

Other devices from Medos International SARL

See all devices from Medos International SARL →

Properties

  • Implantable NoEUDAMEDYesGUDID
  • Reusable
  • CMR Substance
  • Measuring Function
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (17)

  • Sterile: No
  • Single Use: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No