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Traction Tower

by Conmed Corporation 3 variants

Ref 9905A

Traction Tower (9905A) is a Class I device made by Conmed Corporation, registered in EUDAMED on 29 Oct 2025 (Basic UDI-DI 084585465057EE) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10845854026359), 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 Number084585465057EE Basic UDI-DI 10845854026359UDI-DIDate29 Oct 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854026359 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585465057EE registered 29 Oct 2025 Active
  • FDA GUDID UDI-DI 10845854026359 listed 24 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854026359
  2. Registered EUDAMED 084585465057EE

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  • Withdrawn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

Generic name
Intraoperative freestanding patient positioning frame
Device name
Orthopedic, Non-active, Stabilization, Wrist/Arm, Traction Tower, Non-sterile
Model / Ref / Catalog
9905A
Primary DI / UDI-DI
10845854026359
Basic UDI-DI
084585465057EE
Direct marketing DI
20845854026356
FDA product code
FSM
EMDN code
Z12011299 Patient positioning instruments – other
GMDN term
Intraoperative freestanding patient positioning frame
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
US-MF-000012663
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under PATIENT POSITIONING INSTRUMENTS – OTHER.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)