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Perine Nail

EUDAMED

Class I (EU MDR)

Ref KRNG.EL2.1xModel Reusable PERINE guides

by Koelis

Identity

Trade Name
Perine Nail EUDAMED
Device Name
PERINE GRID 14G EUDAMED
Model / Reference
Reusable PERINE guides EUDAMED
KRNG.EL2.1x EUDAMED

Identifiers

Primary DI / UDI-DI
03665134000172 EUDAMED
Basic UDI-DI
3665134PerineGrid_01BN EUDAMED
Direct Marketing DI
03665134000172 EUDAMED
EMDN Code
Z11049080 VARIOUS ULTRASOUND INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

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

Perine Nail by Koelis — Class I — 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
Koelis
EUDAMED SRN
FR-MF-000000830

Sources (1)

  • EUDAMED b2c88b56-9c14-4c7d-8eb6-16d791b5f765 61 fields · synced May 23, 2026