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PureLine - C2F6 Pure

EUDAMED

Class IIb (EU MDR)

Ref VRG310

by Micromed srl

Identity

Trade Name
PureLine - C2F6 Pure EUDAMED
Device Name
Microgas EUDAMED
Model / Reference
VRG310 EUDAMED

Identifiers

Primary DI / UDI-DI
08033757393103 EUDAMED
Basic UDI-DI
803375739MICROGAS97 EUDAMED
EMDN Code
Q02030101 INTRAOCULAR FLUORINATED DERIVATIVES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

PureLine - C2F6 Pure by Micromed srl — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Micromed srl
EUDAMED SRN
IT-MF-000009198

Sources (1)

  • EUDAMED 698ec275-f784-435a-880a-ba34eb1d8c78 61 fields · synced Jul 10, 2026