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Vectra

EUDAMED

Class IIb (EU MDR)

Ref 450.555Model VECTRA-T Plate

by Synthes GmbH

Identity

Trade Name
VECTRA EUDAMED
Device Name
VECTRA-T plate 1 segment 2 segments 3 segments 4 segments EUDAMED
Model / Reference
VECTRA-T Plate EUDAMED
450.555 EUDAMED

Identifiers

Primary DI / UDI-DI
07611819789098 EUDAMED
Basic UDI-DI
7611819a00501JB EUDAMED
EMDN Code
P09070301 CERVICAL FIXATION SYSTEMS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

Yes

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: Cervical spine immobilization system, single-use

Vectra by Synthes GmbH — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cervical spine immobilization system, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Synthes GmbH
EUDAMED SRN
CH-MF-000013345
Authorised Representative
DePuy Ireland UC IE-AR-000009328

Sources (1)

  • EUDAMED 62540073-d97c-4e96-b8fd-b4d502b2c4b8 61 fields · synced Jun 18, 2026