← Back to catalogue

Midline Vascular Access Kit

EUDAMED

Class I (EU MDR)

Ref 061PC04201A

by ITL Asia Pacific Sdn. Bhd.

Identity

Trade Name
Midline Vascular Access Kit EUDAMED
Device Name
Procedure Pack EUDAMED
Model / Reference
061PC04201A EUDAMED

Identifiers

Primary DI / UDI-DI
09555240405975 EUDAMED
Basic UDI-DI
955524040PP1SH3 EUDAMED
EMDN Code
V0599 CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED

Clinical & Handling

Sterile

Yes

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: Ophthalmic surgical procedure kit, non-medicated, single-use

Midline Vascular Access Kit by Itl Asia Pacific Sdn. Bhd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical procedure kit, non-medicated, single-use.

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
MY-MF-000001570
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 019fcc0e-6b77-4313-9809-faf81eb9e491 61 fields · synced Jul 16, 2026