← Back to catalogue

Sapphire 3

EUDAMED

Class III (EU MDR)

Ref 235-303-6Model Ø 3.5 x 30 mm

by OrbusNeich Medical, B.V.

Identity

Trade Name
Sapphire 3 EUDAMED
Device Name
Sapphire 3 EUDAMED
Model / Reference
Ø 3.5 x 30 mm EUDAMED
235-303-6 EUDAMED

Identifiers

Primary DI / UDI-DI
08719244951000 EUDAMED
Basic UDI-DI
B-08719244951000 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
NL-MF-000010907

Sources (1)

  • EUDAMED 96e2bf47-125b-49cf-8091-7f837bf61445 61 fields · synced Jun 19, 2026