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Seigla LiquID Guide Catheter Extension - HSA Registration DE0508792

Access comprehensive regulatory information for Seigla LiquID Guide Catheter Extension in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0508792 and owned by Seigla Medical Inc.. The device was registered on December 27, 2023.

This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.

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CLASS D
DE0508792
Seigla LiquID Guide Catheter Extension
HSA Registration Number: DE0508792
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Product Description

The LiquID Guide Catheter Extension is intended to be used in conjunction with guide catheters to access discrete regions of the coronary and/or peripheral vasculature, and to facilitate placement of interventional devices.

Device Classification
Device Class
CLASS D
Medical Speciality Area
Cardiovascular
Registration Information
Registration Number
DE0508792
Registration Date
December 27, 2023
Retention Due Date
December 26, 2025
Product Owner
Short Name
Seigla Medical Inc.
Address
7688 5th Street SouthEast, Buffalo, Minnesota, United States, 55313, UNITED STATES
Registrant
Address
12A JALAN AMPAS, BALESTIER WAREHOUSE BUILDING, #03-03, SINGAPORE 329516
Importer
Address
12A JALAN AMPAS, BALESTIER WAREHOUSE BUILDING, #03-03, SINGAPORE 329516
Model Information
Model Name(s)
LiquID 061 LiquID 071
Model Identifier(s)
M1000 M2000