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Sapphire 3

EUDAMED

Class III (EU MDR)

Ref 220-103-6Model Ø 2.0 x 10 mm

by OrbusNeich Medical, B.V.

Identity

Trade Name
Sapphire 3 EUDAMED
Device Name
Sapphire 3 EUDAMED
Model / Reference
Ø 2.0 x 10 mm EUDAMED
220-103-6 EUDAMED

Identifiers

Primary DI / UDI-DI
08719244950744 EUDAMED
Basic UDI-DI
B-08719244950744 EUDAMED
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Spain 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

Sapphire 3 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 0cbb3f88-b220-44d7-b012-02b4a4387e37 61 fields · synced Jun 20, 2026