← Back to catalogue

Electric Wheelchair

EUDAMEDFDA UDI

Class I (EU MDR)

Ref BC-EA8003Model BC-EA8000; BC-EA7001; BC-EA8001; BC-EA8002; BC-EA8003; BC-EA8004; BC-EA8005; BC-EA8006; BC-EA8007; BC-EA8008; BC-EA8009; BC-EA8010; BC-EA9000; BC-EA5521; BC-EC01;BC-EC02;BC-EA5515; BC-EA530; BC-EA5513; BC-EALD3; BC-ES6001; BC-ES6003,etcRef BC-EALD3

by Ningbo Baichen Medical Devices Co., Ltd.

Identity

Trade Name
Baichen FDA UDI
Generic Name
Electric-motor-driven wheelchair, occupant-controlled FDA UDI
Device Name
Electric Wheelchair EUDAMED
Model / Reference
BC-EA8000; BC-EA7001; BC-EA8001; BC-EA8002; BC-EA8003; BC-EA8004; BC-EA8005; BC-EA8006; BC-EA8007; BC-EA8008; BC-EA8009; BC-EA8010; BC-EA9000; BC-EA5521; BC-EC01;BC-EC02;BC-EA5515; BC-EA530; BC-EA5513; BC-EALD3; BC-ES6001; BC-ES6003,etc EUDAMED
BC-EA8003 EUDAMED
BC-EALD3 EUDAMEDFDA UDI
Sonix FDA UDI

Identifiers

Primary DI / UDI-DI
06975185620043 EUDAMEDFDA UDI
06975185620142 EUDAMEDFDA UDI
Basic UDI-DI
697518562ewheelchair001YK EUDAMED
510(k) Number
K250475 FDA UDI
FDA Product Code
ITI FDA UDI
EMDN Code
Y122127 ELECTRIC WHEELCHAIRS EUDAMED
GMDN Term
Electric-motor-driven wheelchair, occupant-controlled FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
890.3860 FDA UDI
Market of Registration
Austria 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Electric Wheelchair by Ningbo Baichen Medical Devices Co., Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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-000021409
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (4)

  • EUDAMED fc82214c-ded4-416d-bbee-4988c81c52ca 61 fields · synced Sep 17, 2026
  • EUDAMED ad3ae7eb-e14a-4dd6-b24b-b7da62ef1f4a 61 fields · synced May 18, 2026
  • FDA UDI 3fbe832e-9a36-4f74-b32e-ff354f7cd97d 33 fields · synced May 30, 2026
  • FDA UDI 9dfce975-d9e3-44c0-8ddf-dd9517dcc3ca 33 fields · synced May 30, 2026