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Walker

by Hongkong Pishon Medical Equipment Co., Limited 4 variants

Ref RW410-BLModel RW310，RW310-BL，RW310-BU，RW310-GR，RW310-WH，RW310-BK，RW310-SI，RW310-RD，RW310-CP，RW310-PU，RW310-DB，RW310-LB，RW310-BR，RW310-PN，RW310-OR，RW310-YE，RW310-Red，RW310-Purple，RW310-Black，RW310-Green，etc

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

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number04895262504467 UDI-DI Date13 Apr 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number48952625WalkerQ3 Basic UDI-DI 04895262504467UDI-DIDate12 Jun 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

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  • Withdrawn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
Homland
Generic Name
Handgrip disability-assistive walker, non-powered, non-foldable
Device Name
Walker
Model / Reference
RW310，RW310-BL，RW310-BU，RW310-GR，RW310-WH，RW310-BK，RW310-SI，RW310-RD，RW310-CP，RW310-PU，RW310-DB，RW310-LB，RW310-BR，RW310-PN，RW310-OR，RW310-YE，RW310-Red，RW310-Purple，RW310-Black，RW310-Green，etc, RW410-BL
Primary DI / UDI-DI
04895262504467
Basic UDI-DI
48952625WalkerQ3
FDA Product Code
ITJ
EMDN Code
Y120606 Wheeled walker
GMDN Term
Handgrip disability-assistive walker, non-powered, non-foldable
Device Class
Class I
Regulation Number
890.3825
Market of Registration
Austria
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
HK-MF-000047898
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from HongKong Pishon Medical Equipment Co., Limited

See all devices from HongKong Pishon Medical Equipment Co., Limited →

Properties

  • Premarket Exempt
  • Lot / Batch Number

Other properties (22)

  • Sterile: No
  • Single Use: No
  • 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
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No