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FASPLINT Kit

EUDAMED

Class I (EU MDR)

Ref FS 9000RCModel EV 3000

by Tri-Tech Forensics Inc.

Identity

Trade Name
FASPLINT 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
FS 9000RC EUDAMED

Identifiers

Primary DI / UDI-DI
00850012936541 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

FASPLINT 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 89b52bfc-f08a-4245-9cd1-71060cc0a178 61 fields · synced Jun 20, 2026