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Disposable Silicone Foley Catheter Two-way 16Fr

FDA UDI

Class II (US FDA UDI)

by Guangdong Baihe Medical Technology Co., Ltd

Identity

Trade Name
Disposable Silicone Foley Catheter Two-way 16Fr FDA UDI
Generic Name
Indwelling urethral drainage balloon catheter, non-antimicrobial FDA UDI
Model / Reference
050-FX-021640 FDA UDI

Identifiers

Primary DI / UDI-DI
06938634494800 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

Yes

FDA UDI

Category: Indwelling urethral drainage balloon catheter, non-antimicrobial

Disposable Silicone Foley Catheter Two-way 16Fr by Guangdong Baihe Medical Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Indwelling urethral drainage balloon catheter, non-antimicrobial.

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 bea583da-dddb-4ef9-b240-79bbb7d15a0c 33 fields · synced Jun 8, 2026