← Back to catalogue

Power Wheelchair

EUDAMEDFDA 510(k)

Class I (EU MDR)

Ref N5909Model N5513,N5513A,N5515,N5515A,N5516,N5516A, N5516C,W5517,N5517A,N5519,W5521,W5521B, N5525,W5526,W5536,W5536A,W5536B,W5538, W5538D,N5901,W5905,W5905A,W5907, Q50 R Carbon,N5909,N5909A,W5211,W5211B, W5213,W5213C,W5216,W5217,N5909D,W5915B, W5915C,W5915D,N5919510(k) K230964

by Zhejiang Innuovo Rehabilitation Devices Co., Ltd.

Identity

Trade Name
Power Wheelchair EUDAMED
Device Name
Power Wheelchair EUDAMED
Model / Reference
N5513,N5513A,N5515,N5515A,N5516,N5516A, N5516C,W5517,N5517A,N5519,W5521,W5521B, N5525,W5526,W5536,W5536A,W5536B,W5538, W5538D,N5901,W5905,W5905A,W5907, Q50 R Carbon,N5909,N5909A,W5211,W5211B, W5213,W5213C,W5216,W5217,N5909D,W5915B, W5915C,W5915D,N5919 EUDAMED
N5909 EUDAMED

Identifiers

Primary DI / UDI-DI
06978949461524 EUDAMED
Basic UDI-DI
697894946PW001Y3 EUDAMED
EMDN Code
Y122127 ELECTRIC WHEELCHAIRS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Power Wheelchair by Zhejiang Innuovo Rehabilitation Devices Co., Ltd. — Class I — FDA_510K, MDR — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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

Manufacturer

EUDAMED SRN
CN-MF-000008727
FDA Applicant
Zhejiang Innuovo Rehabilitation Devices Co.,Ltd
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (2)

  • EUDAMED fc5c8468-54a0-45fa-8732-4ac5740fc071 85 fields · synced Jun 18, 2026
  • FDA 510(k) K230964 1 fields · synced May 18, 2026