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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Hi-Torque Connect — 9 UDI-DI variants, MDR

MD Atlas
Lake Region Medical (Galway)

Data from EUDAMED, last updated May 24, 2026

Hi-Torque Connect

081634901HTCGW82

9 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Lake Region Medical (Galway)

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 081634901HTCGW82
Device name: Hi-Torque Connect
Device model: 1012587
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Lake Region Medical (Galway)
SRN: IE-MF-000035376
Country: Ireland
Email: regaffairsguidewires@integer.net

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KM0BPC30GJA9RCRE3GC63AEA

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Hi-Torque connect00816349014895
Hi-Torque Connect00816349014901
Hi-Torque Connect00816349014888
Hi-Torque Connect00816349014918
Hi-Torque Connect00816349014925
Hi-Torque Connect00816349014956
Hi-Torque Connect00816349014963
Hi-Torque Connect00816349014949
Hi-Torque Connect00816349014932