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BeneCath®

FDA UDI

Class II (US FDA UDI)

by Hangzhou Jimushi Meditech Co., Ltd.

Identity

Trade Name
BeneCath® FDA UDI
Generic Name
Intermittent urethral drainage catheter, non-antimicrobial, single-use FDA UDI
Model / Reference
NC18MC FDA UDI

Identifiers

Primary DI / UDI-DI
16972624970605 FDA UDI
FDA Product Code
GBM FDA UDI
GMDN Term
Intermittent urethral drainage catheter, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

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

BeneCath® by Hangzhou Jimushi Meditech Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 657547a6-311f-4c94-9527-d6e6b84665e0 32 fields · synced May 30, 2026