← Back to catalogue

Walking Devices, Two-Handed Operation

EUDAMEDFDA UDI

Class I (EU MDR)

Ref RU4032

by Lerado Zhongshan Peaceful Cove Business Trading Co., Ltd.

Identity

Trade Name
Lerado FDA UDI
Generic Name
Handgrip disability-assistive walker, non-powered, foldable FDA UDI
Device Name
Walking Devices, Two-Handed Operation EUDAMED
Model / Reference
RU4032 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
06973134780213 EUDAMEDFDA UDI
Basic UDI-DI
697313478AW001DJ EUDAMED
Direct Marketing DI
06973134780213 EUDAMED
FDA Product Code
ITJ FDA UDI
EMDN Code
Y120699 WALKING DEVICES, TWO-HANDED OPERATION - OTHER EUDAMED
GMDN Term
Handgrip disability-assistive walker, non-powered, foldable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
890.3825 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Walking Devices, Two-Handed Operation by Lerado Zhongshan Peaceful Cove Business Trading Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000012010
Authorised Representative
KOMAS Medical Technology GmbH DE-AR-000045617

Sources (2)

  • EUDAMED d19cb6bb-5721-420d-9ad0-588a7309a194 61 fields · synced Jun 18, 2026
  • FDA UDI 80961168-bc2d-4195-bfa5-891cc5d9f0d0 32 fields · synced May 30, 2026