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Celluma

EUDAMED

Class IIa (EU MDR)

Ref 850523007228Model Celluma iLITE - EU

by BioPhotas, Inc.

Identity

Trade Name
Celluma EUDAMED
Model / Reference
Celluma iLITE - EU EUDAMED
850523007228 EUDAMED

Identifiers

Primary DI / UDI-DI
00850523007228 EUDAMED
Basic UDI-DI
B-00850523007228 EUDAMED
EMDN Code
Z12040202 PHOTOTHERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Celluma by BioPhotas, Inc. — 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

Manufacturer
BioPhotas, Inc.
EUDAMED SRN
US-MF-000013481
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 585eb4d9-aae8-477f-a33e-1025c6f08d4d 61 fields · synced May 23, 2026