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Ba 40602 U R

EUDAMED

Class I (EU MDR)

Ref BA 40602 U RModel SPLINTS

by Bi̇oakti̇f Tibbi̇ Ürünler Ve Tekni̇k Teksti̇l San. Ti̇c. Ltd. Şti̇.

Identity

Trade Name
BA 40602 U R EUDAMED
Device Name
SPLINTS EUDAMED
Model / Reference
SPLINTS EUDAMED
BA 40602 U R EUDAMED

Identifiers

Primary DI / UDI-DI
08682495005801 EUDAMED
Basic UDI-DI
86824950ATELXT EUDAMED
Direct Marketing DI
08682495005801 EUDAMED
EMDN Code
Y060613 WRIST-HAND-FINGERS ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye 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

Ba 40602 U R by Bi̇oakti̇f Tibbi̇ Ürünler Ve Tekni̇k Teksti̇l San. Ti̇c. Ltd. Şti̇. — 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

EUDAMED SRN
TR-MF-000045383

Sources (1)

  • EUDAMED 0e9c7772-2fa2-4de7-a9d8-c70532be6ad4 61 fields · synced Oct 8, 2026