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Thermoclick

FDA UDI

Class II (US FDA UDI)

by T&R Biofab Co., Ltd

Identity

Trade Name
THERMOCLICK FDA UDI
Generic Name
Infrared patient thermometer, skin FDA UDI
Model / Reference
MT-3000 FDA UDI

Identifiers

Catalog Number
MT-3000 FDA UDI
Primary DI / UDI-DI
08800065225781 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infrared patient thermometer, 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Infrared patient thermometer, skin

Thermoclick by T&R Biofab Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, skin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
T&R Biofab Co., Ltd

Sources (1)

  • FDA UDI 4b142654-44c5-4c76-9783-f0730d573544 34 fields · synced Jun 8, 2026