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Freezer Ring ASB0050

by Tecres

Ref ASB0050

Freezer Ring ASB0050 is a Class I device made by Tecres, registered in EUDAMED on 29 Sep 2026 (Basic UDI-DI 80314970612P3) and listed in FDA GUDID since 23 Sep 2022 (UDI-DI 08031497001999), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number80314970612P3 Basic UDI-DI 08031497001999UDI-DIDate29 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08031497001999 UDI-DI Date23 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 80314970612P3 registered 29 Sep 2026 Active
  • FDA GUDID UDI-DI 08031497001999 listed 23 Sep 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08031497001999
  2. Registered EUDAMED 80314970612P3

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  • Withdrawn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
Freezer Ring
Generic name
Orthopaedic cement-chilling device
Model / reference
ASB0050
Primary DI / UDI-DI
08031497001999
Basic UDI-DI
80314970612P3
FDA product code
KDD
EMDN code
K010399 Spinal endotherapy devices - other
GMDN term
Orthopaedic cement-chilling device
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under SPINAL ENDOTHERAPY DEVICES.

Other devices from Tecres

See all devices from Tecres →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)