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Bright Pad Pro

EUDAMED

Class IIa (EU MDR)

Ref GL07

by Zero-Plus International Limited

Identity

Device Name
Bright Pad Pro EUDAMED
Model / Reference
GL07 EUDAMED

Identifiers

Primary DI / UDI-DI
04897112840367 EUDAMED
Basic UDI-DI
B-04897112840367 EUDAMED
EMDN Code
Z12040202 PHOTOTHERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Red-light phototherapy unit, professional

Bright Pad Pro by Zero-Plus International Limited — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Red-light phototherapy unit, professional.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
HK-MF-000018103
Authorised Representative
Globalmind consumer electronics GmbH DE-AR-000014256

Sources (1)

  • EUDAMED d8f1cf23-a320-4f7b-bf47-57ebad18feba 61 fields · synced Jun 18, 2026