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Eurosilicone S.a.s

EUDAMED

Class III (EU MDR)

Ref 802/160NModel ES.802/160N

by Eurosilicone Sas

Identity

Trade Name
EUROSILICONE S.A.S EUDAMED
Device Name
Round Cristalline Paragel Mammary Implant Medium Profile - Natural EUDAMED
Model / Reference
ES.802/160N EUDAMED
802/160N EUDAMED

Identifiers

Primary DI / UDI-DI
03700469716777 EUDAMED
Basic UDI-DI
B-03700469716777 EUDAMED
EMDN Code
P0601010202 BREAST IMPLANTS, ROUND, 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 3d038fc9-fc82-44ed-afdd-4a433733bac2 61 fields · synced Jun 18, 2026