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Teleport

EUDAMED

Class III (EU MDR)

Ref 221-13-2000Model 2.1 x 135 cm Control

by OrbusNeich Medical, B.V.

Identity

Trade Name
Teleport EUDAMED
Device Name
Teleport EUDAMED
Model / Reference
2.1 x 135 cm Control EUDAMED
221-13-2000 EUDAMED

Identifiers

Primary DI / UDI-DI
08719244950263 EUDAMED
Basic UDI-DI
B-08719244950263 EUDAMED
EMDN Code
C0104020205 PHARMACEUTICAL INFUSION AND ADMINISTRATION INTRAVASCULAR CATHETERS AND MICROCATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Teleport by OrbusNeich Medical, B.V. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
NL-MF-000010907

Sources (1)

  • EUDAMED 9bcdaa08-47e7-499b-b03d-2cffb4833229 61 fields · synced Jun 19, 2026