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Verpal

FDA UDI

Class II (US FDA UDI)

by Anhui JBH Medical Apparatus Co., Ltd.

Identity

Trade Name
VERPAL FDA UDI
Generic Name
Electric-motor-driven wheelchair, occupant-controlled FDA UDI
Model / Reference
DC01 FDA UDI

Identifiers

Catalog Number
DC01 FDA UDI
Primary DI / UDI-DI
06973175530464 FDA UDI
510(k) Number
K212092 FDA UDI
FDA Product Code
ITI FDA UDI
GMDN Term
Electric-motor-driven wheelchair, occupant-controlled FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electric-motor-driven wheelchair, occupant-controlled

Verpal by Anhui JBH Medical Apparatus Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric-motor-driven wheelchair, occupant-controlled.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8e57a469-3df8-472a-8826-95bb6f28f26b 34 fields · synced Jun 1, 2026