← Back to catalogue

Stilea

EUDAMED

Class III (EU MDR)

Ref SkinPlus-HYAL 100JCRef SkinPlus-HYAL 100BCRef SkinPlus-HYAL 100

by BioPlus Co., Ltd.

Identity

Trade Name
Stilea EUDAMED
Device Name
Stilea EUDAMED
Model / Reference
SkinPlus-HYAL 100JC EUDAMED
SkinPlus-HYAL 100BC EUDAMED
SkinPlus-HYAL 100 EUDAMED

Identifiers

Primary DI / UDI-DI
08809639784105 EUDAMED
08809639784167 EUDAMED
08809639784044 EUDAMED
Basic UDI-DI
B-08809639784105 EUDAMED
B-08809639784167 EUDAMED
B-08809639784044 EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye 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

Stilea by BioPlus 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

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

Manufacturer

Manufacturer
BioPlus Co., Ltd.
EUDAMED SRN
KR-MF-000008618
Authorised Representative
KTR Europe GmbH DE-AR-000005685

Sources (3)

  • EUDAMED 1472c8ba-f194-49e8-a6f9-c8616d14aa5e 61 fields · synced Aug 4, 2026
  • EUDAMED 49fbe38f-77f1-4c0f-9396-52f336051d56 61 fields · synced May 17, 2026
  • EUDAMED cd202967-d0d8-49ba-9e03-55f0e5c9ea76 61 fields · synced May 18, 2026