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Prostrolane Inner B SE

EUDAMED

Class III (EU MDR)

Ref N/AModel Prostrolane Inner B SE

by Caregen Co., Ltd.

Identity

Trade Name
Prostrolane Inner B SE EUDAMED
Device Name
Dermal Filler EUDAMED
Model / Reference
Prostrolane Inner B SE EUDAMED
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
08809171381299 EUDAMED
08809171389240 EUDAMED
Basic UDI-DI
B-08809171381299 EUDAMED
B-08809171389240 EUDAMED
EMDN Code
Y062703 AESTHETIC FILLERS, CALF AND THIGH EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Italy EUDAMED
Spain EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

Prostrolane Inner B SE by Caregen Co., Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Caregen Co., Ltd.
EUDAMED SRN
KR-MF-000009948
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 53259983-364a-40bb-9dc1-22aa8141576f 61 fields · synced Jul 18, 2026
  • EUDAMED 52e5482f-b312-473a-908b-49b508d2ec10 61 fields · synced May 19, 2026