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Conmed NS.0011

by Conmed Corporation

Ref NS.0011

Conmed NS.0011 is a Class I device made by Conmed Corporation, registered in EUDAMED on 1 May 2026 (Basic UDI-DI B-10845854027981) and listed in FDA GUDID since 7 Oct 2021 (UDI-DI 10845854027981), active as of 23 Oct 2026.

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

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10845854027981 Basic UDI-DI 10845854027981UDI-DIDate1 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854027981 UDI-DI Date7 Oct 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854027981 registered 1 May 2026 Active
  • FDA GUDID UDI-DI 10845854027981 listed 7 Oct 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854027981
  2. Registered EUDAMED B-10845854027981

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Conmed
Generic name
Intraoperative freestanding patient positioning frame
Device name
Shutt Universal Stress Post Foam Insert
Model / Ref / Catalog
NS.0011
Primary DI / UDI-DI
10845854027981
Basic UDI-DI
B-10845854027981
FDA product code
FWZ
EMDN code
Z12011299 Patient positioning instruments – other
GMDN term
Intraoperative freestanding patient positioning frame
Device class
Class I
Regulation number
878.4950
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Related devices

Category: Intraoperative freestanding patient positioning frame

Similar devices

Also classified as Intraoperative freestanding patient positioning frame.

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

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)