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BM Hydrophilic Nelaton Catheters

EUDAMED

Class I (EU MDR)

Ref 31108002Model Super lubricath catheter:Male,40cm,6Fr,8Fr,10Fr,12Fr,14Fr,16Fr,18Fr,20Fr,22Fr;Female,20cm,6Fr,8Fr,10Fr,12Fr,14Fr,16Fr,18Fr,20Fr,22Fr

by Bonree Medical Co., Ltd.

Identity

Trade Name
BM Hydrophilic Nelaton Catheters EUDAMED
Device Name
Nelaton Catheters EUDAMED
Model / Reference
Super lubricath catheter:Male,40cm,6Fr,8Fr,10Fr,12Fr,14Fr,16Fr,18Fr,20Fr,22Fr;Female,20cm,6Fr,8Fr,10Fr,12Fr,14Fr,16Fr,18Fr,20Fr,22Fr EUDAMED
31108002 EUDAMED

Identifiers

Primary DI / UDI-DI
06942382611785 EUDAMED
Basic UDI-DI
697209192NLTL23QM EUDAMED
Direct Marketing DI
06942382611785 EUDAMED
EMDN Code
U01010501 NELATON CATHETERS, SELF-LUBRICATING EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Category: Intermittent urethral drainage catheter, non-antimicrobial, single-use

BM Hydrophilic Nelaton Catheters by Bonree Medical Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent urethral drainage catheter, non-antimicrobial, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000017844
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 0315f9fd-202a-4ade-8db4-d698f2b08a1a 61 fields · synced Jul 10, 2026