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"Livehold" waste collection bag (unsterilized) - Taiwan Registration 0c6e435e56b3c6388e56f8bccfebd081

Access comprehensive regulatory information for "Livehold" waste collection bag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0c6e435e56b3c6388e56f8bccfebd081 and manufactured by Amedifact Co., Ltd.. The authorized representative in Taiwan is SUNPHORIA 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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0c6e435e56b3c6388e56f8bccfebd081
Registration Details
Taiwan FDA Registration: 0c6e435e56b3c6388e56f8bccfebd081
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Device Details

"Livehold" waste collection bag (unsterilized)
TW: "ๆดปๅฒณ" ๅปขๆถฒๆ”ถ้›†่ข‹ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

0c6e435e56b3c6388e56f8bccfebd081

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of classification and grading management of medical equipment, "Non-powered, single-patient, portable suction equipment (I.4680)".

I General, Plastic Surgery and Dermatology

I.4680 Non-motive, single patient-use, carry-on suctioning device

Domestic;; Contract manufacturing

Dates and Status

Jul 09, 2018

Jul 09, 2028