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Jbh

FDA UDI

Class II (US FDA UDI)

by Anhui JBH Medical Apparatus Co., Ltd.

Identity

Trade Name
JBH FDA UDI
Generic Name
Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible FDA UDI
Model / Reference
D09 FDA UDI

Identifiers

Primary DI / UDI-DI
06973175532314 FDA UDI
510(k) Number
K170787 FDA UDI
FDA Product Code
ITI FDA UDI
GMDN Term
Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible

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

Similar devices

Also classified as Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible.

Cleared under the same submission

K170787 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Anhui JBH Medical Apparatus Co., Ltd.

Sources (1)

  • FDA UDI 7797d64a-e37a-4ef1-8034-2c2f556f3032 33 fields · synced May 30, 2026