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Medstone Combination Patient Arm Board

by Stille AB

Ref 505-1112Model 505-1110, 505-1112, 505-1118, 535-1730

Medstone Combination Patient Arm Board (505-1112) is a fluoroscopy/angiography table (EU MDR Class I; FDA Class I; FDA product code GDC, Table, Operating-Room, Electrical) made by Stille AB, registered in EUDAMED on 20 Mar 2025 (Basic UDI-DI 73323395002P7) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 07332339222253), 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 Number73323395002P7 Basic UDI-DI 07332339222253UDI-DIDate20 Mar 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number07332339222253 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 73323395002P7 registered 20 Mar 2025 Active
  • FDA GUDID UDI-DI 07332339222253 listed 24 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07332339222253
  2. Registered EUDAMED 73323395002P7

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  • Withdrawn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
Combination Patient Armboard EUDAMED
Medstone GUDID
Generic name
Fluoroscopy/angiography table, powered
Device name
Armboard
Model / Ref / Catalog
505-1110, 505-1112, 505-1118, 535-1730, Combination Patient Arm Board
Primary DI / UDI-DI
07332339222253
Basic UDI-DI
73323395002P7
Direct marketing DI
07332339222253
FDA product code
GDC
EMDN code
Z12011280 Patient positioning instruments - hardware accessories
GMDN term
Fluoroscopy/angiography table, powered
Device class
Class I
Regulation number
878.4960
EU registration type
Standard device
EU market of registration
Sweden
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
505-1110, 505-1112, 505-1118, 535-1730
505-1112
GUDID
Combination Patient Arm Board

Related devices

Category: Fluoroscopy/angiography table, powered

Similar devices in this category

Other devices filed under PATIENT POSITIONING INSTRUMENTS - HARDWARE ACCESSORIES.

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Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)