← Back to catalogue

MixJect

EUDAMED

Class IIa (EU MDR)

Ref 9070012

by West Pharma. Services IL, Ltd.

Identity

Trade Name
MixJect EUDAMED
Device Name
MixJect® EUDAMED
Model / Reference
9070012 EUDAMED

Identifiers

Primary DI / UDI-DI
07290108241457 EUDAMED
Basic UDI-DI
729010824MJTDCR EUDAMED
EMDN Code
A019099 NEEDLES FOR OTHER PROCEDURES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

MixJect by West Pharma. Services IL, Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

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
IL-MF-000008572
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 0ef5e598-49c2-4def-8b64-bcf35b262e8b 61 fields · synced Jul 28, 2026