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Disposable Silicone Foley Catheter

FDA UDI

Class II (US FDA UDI)

by Guangdong Baihe Medical Technology Co., Ltd

Identity

Trade Name
Disposable Silicone Foley Catheter FDA UDI
Generic Name
Indwelling urethral drainage balloon catheter, non-antimicrobial FDA UDI
Model / Reference
Three-way 20Fr FDA UDI

Identifiers

Catalog Number
FX-032040 FDA UDI
Primary DI / UDI-DI
06938634494916 FDA UDI
510(k) Number
K130908 FDA UDI
FDA Product Code
EZL FDA UDI
GMDN Term
Indwelling urethral drainage balloon catheter, non-antimicrobial 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

No

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: Indwelling urethral drainage balloon catheter, non-antimicrobialIndwelling urethral catheterization kit, adult

Disposable Silicone Foley Catheter by Guangdong Baihe Medical Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Indwelling urethral catheterization kit, adult.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9cefa688-c0e3-436d-9a2c-c8c2ce6cba99 34 fields · synced May 30, 2026