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Jj

FDA UDI

Class I (US FDA UDI)

by Yangzhou Jiwei Sports Products CO., LTD

Identity

Trade Name
JJ FDA UDI
Generic Name
Knee support orthosis FDA UDI
Model / Reference
Small FDA UDI

Identifiers

Primary DI / UDI-DI
16935012800014 FDA UDI
FDA Product Code
IQI FDA UDI
GMDN Term
Knee support orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Knee support orthosis

Jj by Yangzhou Jiwei Sports Products CO., LTD — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee support orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5a98f57a-e840-4bf7-9cdc-56da57c04789 32 fields · synced May 30, 2026