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Preve

FDA UDIEUDAMED

Class II (US FDA UDI)

by Guangzhou Berrcom Medical Device Co., Ltd

Identity

Trade Name
PREVE FDA UDI
Generic Name
Infrared patient thermometer, skin FDA UDI
Model / Reference
JXB-313 FDA UDI

Identifiers

Primary DI / UDI-DI
06947656112531 FDA UDI
FDA Product Code
FLL FDA UDI
SDV 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Infrared patient thermometer, skin

Preve by Guangzhou Berrcom Medical Device Co., Ltd — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, skin.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 7862e5b5-e412-4dad-b9ed-8f7eb8d09c11 32 fields · synced May 30, 2026
  • EUDAMED 1 fields · synced May 22, 2026