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HandStand™

by Conmed Corporation United States EUDAMEDGUDID

Ref HS-FS, HS-TT, HS-DT2, HS-KIT10, HS-BS

Product code FSMEMDN K0301

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number084585408761DT Basic UDI-DIDate2 Feb 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number084585408761DT Basic UDI-DIDate2 Feb 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854051504 UDI-DIDate23 Nov 2020ListedStatusIn distribution

Coverage

2 jurisdictions

United States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaSwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Listed
  • Not covered
  • European Union CE/MDD, CE/MDR Active
  • United States GUDID listing Listed

Recalls: none on record (FDA, checked 22 Oct 2026)

Certificates: none listed in EUDAMED

Specification

EUDAMED · GUDID · synced 22 Oct 2026

Generic Name
Upper-limb traction wrap/trap, single-use
Intraoperative freestanding patient positioning frame
Device Name
Orthopedic, Non-active, Stabilization, Hand, Sterile
Orthopedic, Non-active, Stabilization, Wrist/Arm, Traction Tower, Non-sterile
Model / Ref / Catalog
HS-FS, HS-TT, HS-DT2, HS-KIT10, HS-BS
Primary DI / UDI-DI
10845854051504, 10845854051535, 10845854051481, 10845854051528, 10845854051511
Basic UDI-DI
084585408761DT, 084585465057EE, B-10845854051528
Unit of Use DI
00845854051484
Direct Marketing DI
20845854051532
FDA Product Code
FSM
EMDN Code
K0301, Z12011299
GMDN Term
Upper-limb traction wrap/trap, single-use
Intraoperative freestanding patient positioning frame
Device Class
Class I
Regulation Number
878.4800
Market of Registration
Belgium
Commercial Distribution
In Commercial Distribution
Sterilization Method
Radiation Sterilization
Moist Heat or Steam Sterilization

Manufacturer details

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

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile NoEUDAMEDGUDIDYesEUDAMEDGUDID
  • Single Use YesGUDIDNoGUDID
  • Prescription Use
  • Convenience Kit NoGUDIDYesGUDID
  • Premarket Exempt
  • Lot / Batch Number YesGUDIDNoGUDID
  • Serial Number NoGUDIDYesGUDID
  • Expiration Date YesGUDIDNoGUDID
  • Manufacturing Date NoGUDIDYesGUDID
Other properties (15)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No

Sources (10)

  • EUDAMED 07eff01b-4943-4406-9e4a-89432677c402 61 fields · synced 22 Oct 2026
  • EUDAMED 10845854051535|084585465057EE 61 fields · synced 17 May 2026
  • EUDAMED 10845854051481|084585408761DT 61 fields · synced 17 May 2026
  • EUDAMED 10845854051528|B-10845854051528 61 fields · synced 18 May 2026
  • EUDAMED 10845854051511|084585408761DT 61 fields · synced 19 May 2026
  • FDA UDI 0ed29217-7e04-4e0d-a258-ca1d0c6ae276 36 fields · synced 30 May 2026
  • FDA UDI 5f013fd4-c813-46e8-aa86-d751f4ff6f7c 36 fields · synced 30 May 2026
  • FDA UDI b4b3c557-b8c2-40f6-9ef1-1fffff2fa9f6 36 fields · synced 30 May 2026
  • FDA UDI 6aa93761-9be1-424a-ae48-0d41f14e7145 36 fields · synced 30 May 2026
  • FDA UDI e20eb8ee-dc7a-4702-8f4c-1b73924005ab 36 fields · synced 30 May 2026