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Eurosilicone S.a.s

EUDAMED

Class III (EU MDR)

Ref TMF2/250Model ES.TMF2/250

by Eurosilicone Sas

Identity

Trade Name
EUROSILICONE S.A.S EUDAMED
Device Name
Anatomical Cristalline Paragel Mammary Implant - The Matrix - High Profile - Medium Projection EUDAMED
Model / Reference
ES.TMF2/250 EUDAMED
TMF2/250 EUDAMED

Identifiers

Primary DI / UDI-DI
03700469716074 EUDAMED
Basic UDI-DI
B-03700469716074 EUDAMED
EMDN Code
P0601020202 BREAST IMPLANTS, ANATOMICAL, MADE OF SILICONE, WITH TEXTURED SURFACE EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
France 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

Eurosilicone S.a.s by Eurosilicone Sas — 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
Eurosilicone Sas
EUDAMED SRN
FR-MF-000008947

Sources (1)

  • EUDAMED bf6d8baa-3e7a-429c-9e24-9528cd25c1df 61 fields · synced Jun 18, 2026