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Polyamide

EUDAMED

Class III (EU MDR)

Ref JN02HR40

by Gmd Group Medi̇kal Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

Identity

Trade Name
POLYAMIDE EUDAMED
Device Name
PA MONOFILAMENT EMİLEMEYEN SÜTÜR 75cm 2 SİYAH 40mm 1/2 DAİRE YUVARLAK İĞNE EUDAMED
Model / Reference
JN02HR40 EUDAMED

Identifiers

Primary DI / UDI-DI
D-08681677082692XP EUDAMED
Basic UDI-DI
B-08681677082692XP EUDAMED
EMDN Code
H010201010101 POLYAMIDE MONOFILAMENT WITH NEEDLE EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

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

Polyamide by Gmd Group Medi̇kal Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ — 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

EUDAMED SRN
TR-MF-000030794

Sources (1)

  • EUDAMED 82a0e007-5df0-4549-a525-932abfcec51c 61 fields · synced Oct 6, 2026