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"Hanmo" inflatable tourniquet (unsterilized) - Taiwan Registration 2bae5e251bc16cdc5a7e4170aa4fd1bd

Access comprehensive regulatory information for "Hanmo" inflatable tourniquet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2bae5e251bc16cdc5a7e4170aa4fd1bd and manufactured by HAMMARPLAST MEDICAL AB. The authorized representative in Taiwan is MEDISOL ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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2bae5e251bc16cdc5a7e4170aa4fd1bd
Registration Details
Taiwan FDA Registration: 2bae5e251bc16cdc5a7e4170aa4fd1bd
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Device Details

"Hanmo" inflatable tourniquet (unsterilized)
TW: โ€œๆถต่Žซโ€ๅ……ๆฐฃๅผๆญข่ก€ๅธถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2bae5e251bc16cdc5a7e4170aa4fd1bd

DHA04401252101

Company Information

Sweden

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Inflatable Tourniquet (I.5910)".

I General, Plastic Surgery and Dermatology

I.5910 ๅ……ๆฐฃๅผๆญข่ก€ๅธถ

import

Dates and Status

Dec 25, 2012

Dec 25, 2022

Apr 12, 2024

Cancellation Information

Logged out

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