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Marketlab Inc

FDA UDI

Class II (US FDA UDI)

by Marketlab Inc.

Identity

Trade Name
Marketlab Inc FDA UDI
Generic Name
Indwelling urethral drainage balloon catheter, non-antimicrobial FDA UDI
Device Name
30cc/24Fr 100% Silicone Foley Catheter PK12 FDA UDI
Model / Reference
42468 FDA UDI
Description
30cc/24Fr 100% Silicone Foley Catheter PK12 FDA UDI

Identifiers

Catalog Number
42468 FDA UDI
Primary DI / UDI-DI
00817517020762 FDA UDI
510(k) Number
K160235 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Indwelling urethral drainage balloon catheter, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

Yes

FDA UDI

Convenience Kit

Yes

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-antimicrobial

Marketlab Inc by Marketlab Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Manufacturer
Marketlab Inc.

Sources (1)

  • FDA UDI 1a61c0d5-4cec-4c4d-9aee-7cc24bfb6ad4 36 fields · synced Jun 7, 2026