UMBILI-CATH - A Single-Lumen Silicone Umbilical Catheter, 3.5 - UTAH MEDICAL PRODUCTS, INC.

Duns Number:094651270

Device Description: A Single-Lumen Silicone Umbilical Catheter, 3.5 French

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More Product Details

Catalog Number

4173505

Brand Name

UMBILI-CATH

Version/Model Number

Single-Lumen Silicone

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K940953,K940953

Product Code Details

Product Code

FOS

Product Code Name

Catheter, Umbilical Artery

Device Record Status

Public Device Record Key

7151626f-356a-4562-b59c-d15ad83228f0

Public Version Date

December 18, 2019

Public Version Number

4

DI Record Publish Date

September 23, 2016

Additional Identifiers

Package DI Number

H67140735051

Quantity per Package

10

Contains DI Package

H67141735050

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"UTAH MEDICAL PRODUCTS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 35
2 A medical device with a moderate to high risk that requires special controls. 274