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MyPLLA

EUDAMED

Class III (EU MDR)

Ref Not applicableModel MyPLLA

by PRP Science Co., Ltd.

Identity

Trade Name
MyPLLA EUDAMED
Device Name
Sterile Absorbable Poly-L-Lactic acid (PLLA) Dermal Filler EUDAMED
Model / Reference
MyPLLA EUDAMED
Not applicable EUDAMED

Identifiers

Primary DI / UDI-DI
08800125100478 EUDAMED
Basic UDI-DI
B-08800125100478 EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Ireland 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

MyPLLA by PRP Science 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

EUDAMED SRN
KR-MF-000014450
Authorised Representative
Meridius Medical Europe Limited IE-AR-000004258

Sources (1)

  • EUDAMED f14597e3-83bb-402c-943e-b2c36fee8c07 61 fields · synced Jun 20, 2026