← Back to catalogue

Ba 913 Xl

EUDAMED

Class I (EU MDR)

Ref BA 913 XLModel FOOT HEALTH SUPPORT

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

Identity

Trade Name
BA 913 XL EUDAMED
Device Name
FOOT HEALTH SUPPORT PRODUCTS EUDAMED
Model / Reference
FOOT HEALTH SUPPORT EUDAMED
BA 913 XL EUDAMED

Identifiers

Primary DI / UDI-DI
08682495012175 EUDAMED
Basic UDI-DI
86824950AYAKURUNLERISE EUDAMED
Direct Marketing DI
08682495012175 EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT 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

Category: Ankle/foot orthosis

Ba 913 Xl by Bi̇oakti̇f Tibbi̇ Ürünler Ve Tekni̇k Teksti̇l San. Ti̇c. Ltd. Şti̇. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
TR-MF-000045383

Sources (1)

  • EUDAMED e33e4db8-164a-4b10-8b82-0d7a9d323a7d 61 fields · synced Jul 30, 2026