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Amplatz Renal Dilation Set - S

EUDAMED

Class IIa (EU MDR)

Ref BAR0630000SE

by Blue Neem Medical Devices Private Limited

Identity

Trade Name
Amplatz Renal Dilation Set - S EUDAMED
Device Name
Percutaneous Dilators EUDAMED
Model / Reference
BAR0630000SE EUDAMED

Identifiers

Primary DI / UDI-DI
08905080010562 EUDAMED
Basic UDI-DI
8905080BPDGH EUDAMED
EMDN Code
U03010101 AMPLATZ CANNULAS FOR URINARY DILATION EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

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

Amplatz Renal Dilation Set - S by Blue Neem Medical Devices Private Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IN-MF-000021793
Authorised Representative
Arazy Group (Ireland) Ltd. IE-AR-000000093

Sources (1)

  • EUDAMED f353d9eb-ea09-4537-8229-efe012dc064c 61 fields · synced Oct 7, 2026