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Femoral distal augment trial , RM/LL , #3 , 8mm

EUDAMED

Class I (EU MDR)

Ref NMRKS099Model TRIALS

by Normmed Medi̇kal San. Ve Ti̇c. A.ş.

Identity

Trade Name
Femoral distal augment trial , RM/LL , #3 , 8mm EUDAMED
Model / Reference
TRIALS EUDAMED
NMRKS099 EUDAMED

Identifiers

Primary DI / UDI-DI
08682549539405 EUDAMED
Basic UDI-DI
86804870TLHT EUDAMED
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Surgical retraction system, reusable

Femoral distal augment trial , RM/LL , #3 , 8mm by Normmed Medi̇kal San. Ve Ti̇c. A.ş. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TR-MF-000015713

Sources (1)

  • EUDAMED 0344d663-488c-41c9-b6e5-f8f9cb55a3dd 61 fields · synced Jul 31, 2026