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PureLine - C3F8 Pure

EUDAMED

Class IIb (EU MDR)

Ref VRG320

by Micromed srl

Identity

Trade Name
PureLine - C3F8 Pure EUDAMED
Device Name
Microgas EUDAMED
Model / Reference
VRG320 EUDAMED

Identifiers

Primary DI / UDI-DI
08033757393202 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 - C3F8 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 638a0aac-8707-40c3-866d-d9edf8b7efc0 61 fields · synced Jul 16, 2026