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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 catheterization kit, adult FDA UDI
Model / Reference
Two-way 8Fr FDA UDI

Identifiers

Catalog Number
FX-020831 FDA UDI
Primary DI / UDI-DI
06938634484153 FDA UDI
510(k) Number
K130908 FDA UDI
FDA Product Code
EZL FDA UDI
GMDN Term
Indwelling urethral catheterization kit, adult 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 7903ebb9-43f9-41c7-8169-9e0a57a12b71 34 fields · synced Jun 1, 2026