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Phs

by medica Medizintechnik GmbH 2 variants

Part of a family of 6 devices: see the family page

Ref A008-688

Phs (A008-688) is a device classified as Class I in the EU and Class II in the US made by medica - Medizintechnik GmbH, registered in EUDAMED on 12 Nov 2025 (Basic UDI-DI 4041925PHSBQ) and listed in FDA GUDID since 14 Nov 2024 (UDI-DI 04041925006148), withdrawn (EUDAMED), not in commercial distribution (GUDID) as of 23 Oct 2026.

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

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 Number4041925PHSBQ Basic UDI-DI 04041925006148UDI-DIDate12 Nov 2025RegisteredStatusWithdrawn No longer placed on the EU market
United StatesGUDID listing GUDID Number04041925006148 UDI-DI Date14 Nov 2024ListedStatusListed GUDID: not in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4041925PHSBQ registered 12 Nov 2025 Withdrawn
  • FDA GUDID UDI-DI 04041925006148 listed 14 Nov 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04041925006148
  2. Registered EUDAMED 4041925PHSBQ

Coverage

2 jurisdictions

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  • Withdrawn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  • European Union CE/MDR Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Phs - L
Generic name
General-purpose patient lifting system sling/harness
Device name
Phs
Model / Ref / Catalog
A008-688, GBS 01.YY.ZZ
Primary DI / UDI-DI
04041925006148
Basic UDI-DI
4041925PHSBQ
Direct marketing DI
04041925006148
FDA product code
IKK
EMDN code
Y0580 Learning and training devices - accessories
GMDN term
General-purpose patient lifting system sling/harness
Device class
Class I EUDAMED
Class II GUDID
Regulation number
890.1925
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
Not in Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
A008-688
GUDID
GBS 01.YY.ZZ
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Manufacturer details

EUDAMED SRN
DE-MF-000005058

Similar devices in this category

Other devices filed under ABILITIES LEARNING AND TRAINING DEVICES.

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)