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BD Ready-to-Use Hydrophilic Catheter

EUDAMEDFDA UDI

Class I (EU MDR)

Ref RTU06P

by Hangzhou Bever Medical Devices Co., Ltd.

Identity

Trade Name
BD Ready-to-Use Hydrophilic Catheter EUDAMED
BD Intermittent FDA UDI
Generic Name
Single-administration urethral drainage catheter FDA UDI
Device Name
Ready-to-Use Hydrophilic Catheter EUDAMED
BD Ready-To-Use Hydrophilic Catheter FDA UDI
Model / Reference
RTU06P EUDAMEDFDA UDI
Description
BD Ready-To-Use Hydrophilic Catheter FDA UDI

Identifiers

Catalog Number
RTU06P FDA UDI
Primary DI / UDI-DI
06948796204018 EUDAMEDFDA UDI
Basic UDI-DI
69487962NC0003Q8 EUDAMED
510(k) Number
K192468 FDA UDI
FDA Product Code
GBM FDA UDI
EZD FDA UDI
EMDN Code
U01010501 NELATON CATHETERS, SELF-LUBRICATING EUDAMED
GMDN Term
Single-administration urethral drainage catheter FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
876.5130 FDA UDI
Market of Registration
Poland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 6 French FDA UDI
Catheter Length — 10 Inch FDA UDI

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

BD Ready-to-Use Hydrophilic Catheter by Hangzhou Bever Medical Devices Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
CN-MF-000018408
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (3)

  • EUDAMED 544a7bf5-3be5-4f7a-acaf-b5af56781dff 61 fields · synced Jun 19, 2026
  • FDA UDI 2387852c-f685-4e0f-952b-1ca633eccb4a 37 fields · synced May 30, 2026
  • EUDAMED 4e68894c-8723-43c9-ba1f-251ce381a34f 61 fields · synced Jun 19, 2026