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Cofoe

FDA UDI

Class I (US FDA UDI)

by Cofoe Medical Technology Co., Ltd.

Identity

Trade Name
Cofoe FDA UDI
Generic Name
Walker tray FDA UDI
Device Name
Walker FDA UDI
Model / Reference
KFZXJ003 FDA UDI
Description
Walker FDA UDI

Identifiers

Primary DI / UDI-DI
06950715503324 FDA UDI
FDA Product Code
ITJ FDA UDI
GMDN Term
Walker tray FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3825 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: Walker tray

Cofoe by Cofoe Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Walker tray.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 03eb44de-98b1-4ea0-909e-1803a52c72ab 34 fields · synced Jun 8, 2026