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Fiberglass Splint

EUDAMED

Class I (EU MDR)

Ref a+635(150mm×750mm)Model AX315(75mm×300mm)

by Shaanxi Ansen Medical Technology Development Co., Ltd

Identity

Trade Name
Fiberglass Splint EUDAMED
Device Name
Fiberglass Splint EUDAMED
Model / Reference
AX315(75mm×300mm) EUDAMED
a+635(150mm×750mm) EUDAMED

Identifiers

Primary DI / UDI-DI
06970210232536 EUDAMED
Basic UDI-DI
697021023AX0023B EUDAMED
EMDN Code
M03050202 SYNTHETIC CAST BANDAGES AND SPLINTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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: Cotton wool roll, sterile

Fiberglass Splint by Shaanxi Ansen Medical Technology Development Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cotton wool roll, sterile.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000050669
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED 0c850a31-294b-4dca-9aa3-1d65946401d1 61 fields · synced Jun 18, 2026