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Sapphire II PRO

EUDAMED

Class III (EU MDR)

Ref 230-103-5UModel Ø 3.0 x 10 mm

by OrbusNeich Medical, B.V.

Identity

Trade Name
Sapphire II PRO EUDAMED
Device Name
Sapphire II PRO EUDAMED
Model / Reference
Ø 3.0 x 10 mm EUDAMED
230-103-5U EUDAMED

Identifiers

Primary DI / UDI-DI
08717853296840 EUDAMED
Basic UDI-DI
B-08717853296840 EUDAMED
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany 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

Category: Coronary angioplasty balloon catheter, cutting/scoring

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

Similar devices

Also classified as Coronary angioplasty balloon catheter, cutting/scoring.

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 3578aa51-f52f-4536-9776-6bd021ef9cea 61 fields · synced Oct 6, 2026