Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9616675

FEI Number

3003105967

Entity Name

UTAH MEDICAL PRODUCTS, LTD.

City/State/Country

ATHLONE CO. Leinster, IE

Establishment Address

ATHLONE BUSINESS & TECHNOLOGY PARK, DUBLIN ROAD, ATHLONE CO. Leinster --, IE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

UTAH MEDICAL PRODUCTS, INC. (Owner Number: 1718873)

Owner / Operator Contact Address

7043 SOUTH 300 WEST, --, Midvale, UT 84047, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DELTRAN ABC PATHFINDER PLUS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CBT	Arterial Blood Sampling Kit	Anesthesiology	Class 1	868.1100	2007-10-15
FFY	Adaptor, Bulbs, Miscellaneous, For Endoscope	Gastroenterology, Urology	Class 1	876.1500	2006-03-31
KNH	Laparoscopic Contraceptive Tubal Occlusion Device	Obstetrics/Gynecology	Class 3	884.5380	2024-12-10

Official Correspondent

No official correspondent registered.

US Agent Details

Ben Shirley Business: Utah Medical Products Inc. Email: bshirley@utahmed.com Phone: (801) 5661200

Related Public Records

Same Entity

UTAH MEDICAL PRODUCTS, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1718873	UTAH MEDICAL PRODUCTS, INC.	Midvale, UT, US

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0037-2015	Richard Wolf Medical Instruments Corp.	3	The Hulka Clip is a sterile packaged medical device that carries a two year expiration date. It is packaged two clips per procedural tray. Theses procedural trays are then sealed in a Tyvek/Mylar pouch and packaged in a cardboard shipping carton with ten pouches in each shipping carton.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9616675. Last updated year: 2026. Please use registration number 9616675 when referencing this establishment in official correspondence.