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Restore 219309

by Medos International Sàrl

Ref 219309Model General Orthopedic Use Rasps

Restore 219309 is a Class I device made by Medos International Sàrl, registered in EUDAMED on 21 May 2026 (Basic UDI-DI 0886705a00132K9) and listed in FDA GUDID since 1 Sep 2015 (UDI-DI 10886705005642), active as of 23 Oct 2026.

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

CE MDR

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0886705a00132K9 Basic UDI-DI 10886705005642UDI-DIDate21 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10886705005642 UDI-DI Date1 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0886705a00132K9 registered 21 May 2026 Active
  • FDA GUDID UDI-DI 10886705005642 listed 1 Sep 2015 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10886705005642
  2. Registered EUDAMED 0886705a00132K9

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  • Withdrawn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 Curved Rasp EUDAMED
Restore GUDID
Generic name
Bone file/rasp, manual, reusable
Device name
RESTORE, Rasp, Flat, Curved
Model / Ref / Catalog
219309, General Orthopedic Use Rasps
Primary DI / UDI-DI
10886705005642
Basic UDI-DI
0886705a00132K9
Direct marketing DI
10886705005642
FDA product code
NBH
EMDN code
L1920 Arthroscopic surgery files and rasps, reusable
GMDN term
Bone file/rasp, manual, reusable
Device class
Class I
Regulation number
888.1100
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone file/rasp, manual, reusable

Similar devices in this category

Other devices filed under ARTHROSCOPIC SURGERY INSTRUMENTS, REUSABLE.

Other devices from Medos International SARL

See all devices from Medos International SARL →

Properties

  • Sterilise before use
  • Reusable
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (19, all answered No)