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Uri-Cath

FDA UDI

Class II (US FDA UDI)

by Utah Medical Products, Inc.

Identity

Trade Name
URI-CATH FDA UDI
Generic Name
Single-administration urethral drainage catheter FDA UDI
Device Name
Urinary Drainage and Collection Set with a Silicone Urinary Drainage Catheter, 3.5 French FDA UDI
Model / Reference
Silicone Catheter Set FDA UDI
Description
Urinary Drainage and Collection Set with a Silicone Urinary Drainage Catheter, 3.5 French FDA UDI

Identifiers

Catalog Number
4193507 FDA UDI
Primary DI / UDI-DI
H67141935070 FDA UDI
510(k) Number
K941672 FDA UDI
FDA Product Code
GBM FDA UDI
GMDN Term
Single-administration urethral drainage catheter 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

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

Dimensions & Sizes

Size
Length — 34 Centimeter FDA UDI
Catheter Gauge — 3.5 French FDA UDI

Category: Single-administration urethral drainage catheter

Uri-Cath by Utah Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Single-administration urethral drainage catheter.

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 649002c0-18c7-46a2-a2cf-4951f2c71533 37 fields · synced Jun 9, 2026