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Berrcom

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref JXB311+GAR050Model JXB-178, JXB-182, JXB-183, JXB-311, JXB-315, JXB-319, BL-6001, JXB-180, JXB-195, JXB-190, JXB-192, JA001, JXB-301, JXB-302, JXB-182B, JXB-308, JXB-320, LMP001, EW-TA50, EW-TA51

by Guangzhou Berrcom Medical Device Co., Ltd.

Identity

Trade Name
BERRCOM EUDAMEDFDA UDI
Generic Name
Infrared patient thermometer, skin FDA UDI
Device Name
Non-contact Infrared Thermometer EUDAMED
Model / Reference
JXB-178, JXB-182, JXB-183, JXB-311, JXB-315, JXB-319, BL-6001, JXB-180, JXB-195, JXB-190, JXB-192, JA001, JXB-301, JXB-302, JXB-182B, JXB-308, JXB-320, LMP001, EW-TA50, EW-TA51 EUDAMED
JXB311+GAR050 EUDAMED
JXB-311 FDA UDI

Identifiers

Primary DI / UDI-DI
06947656112777 EUDAMEDFDA UDI
Basic UDI-DI
69476561JXB-XXX7T EUDAMED
Direct Marketing DI
06947656112777 EUDAMED
FDA Product Code
FLL FDA UDI
SDV FDA UDI
EMDN Code
V0301010202 NON-CONTACT DIGITAL THERMOMETERS EUDAMED
GMDN Term
Infrared patient thermometer, skin FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
880.2910 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000013852
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED c288094e-5816-4be2-b29a-ce9b532cc0d2 61 fields · synced May 31, 2026
  • FDA UDI 37d8b9fb-d2dd-440c-839c-fb9bfa4af9d1 32 fields · synced May 29, 2026