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Cocet

FDA UDI

Class II (US FDA UDI)

by Kangfu Medical Equipment Factory

Identity

Trade Name
COCET FDA UDI
Generic Name
Infrared patient thermometer, ear/skin FDA UDI
Model / Reference
KFT-28 FDA UDI

Identifiers

Primary DI / UDI-DI
06943532402802 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infrared patient thermometer, ear/skin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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
Sterilization Method
Liquid Chemical FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Infrared patient thermometer, ear/skin

Cocet by Kangfu Medical Equipment Factory — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, ear/skin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fcc90e0a-2290-4720-81c3-c83b8efe0584 32 fields · synced Jun 8, 2026