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EVAC-U-SPLINT Kit

EUDAMED

Class I (EU MDR)

Ref EV 3000

by Tri-Tech Forensics Inc.

Identity

Trade Name
EVAC-U-SPLINT Kit EUDAMED
Device Name
EVAC-U-SPLINT Extremity Splint Set (Small, Medium and Large Splints, Compact Pump, Carry Case) EUDAMED
Model / Reference
EV 3000 EUDAMED

Identifiers

Primary DI / UDI-DI
00850012936411 EUDAMED
Basic UDI-DI
0850012936VKITX6 EUDAMED
EMDN Code
V0804 PATIENT IMMOBILISERS (in diagnostic or therapeutic procedures) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

EVAC-U-SPLINT Kit by Tri-Tech Forensics Inc. — 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
US-MF-000024012
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (1)

  • EUDAMED edc0e130-6023-454d-b97a-fde3f8d15015 61 fields · synced Jul 21, 2026