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Fascial Dilator

EUDAMED

Class IIa (EU MDR)

Ref BFDN0060220S

by Blue Neem Medical Devices Private Limited

Identity

Trade Name
Fascial Dilator EUDAMED
Device Name
Percutaneous Dilators EUDAMED
Model / Reference
BFDN0060220S EUDAMED

Identifiers

Primary DI / UDI-DI
08905080000761 EUDAMED
Basic UDI-DI
8905080BPDGH EUDAMED
EMDN Code
U03010199 PERCUTANEOUS NEPHROSTOMY, SEQUENTIAL DILATORS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia 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

Fascial Dilator by Blue Neem Medical Devices Private Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Manufacturer's product page: View Product >

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 0dd40db7-d346-4004-8660-c5e0e42866c9 61 fields · synced Oct 6, 2026