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"Coloplast" SenSura Mio Ostomy Pouch and Accessories (Non-Sterile) - Taiwan Registration 08955c1c33e009d3191f1da8d30e432f

Access comprehensive regulatory information for "Coloplast" SenSura Mio Ostomy Pouch and Accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 08955c1c33e009d3191f1da8d30e432f and manufactured by COLOPLAST HUNGARY KFT. The authorized representative in Taiwan is COLOPLAST TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including COLOPLAST HUNGARY KFT, and 1 recent registrations in the same category. 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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08955c1c33e009d3191f1da8d30e432f
Registration Details
Taiwan FDA Registration: 08955c1c33e009d3191f1da8d30e432f
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Device Details

"Coloplast" SenSura Mio Ostomy Pouch and Accessories (Non-Sterile)
TW: "ๅบทๆจ‚ไฟ"ๅ–„่ˆ’ๆจ‚ๅฏ†ๅ„ช้€ ๅฃ่ก“็”จ่ข‹ๅŠๅ…ถ้™„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

08955c1c33e009d3191f1da8d30e432f

Ministry of Health Medical Device Import No. 020575

DHA09402057500

Company Information

Hungary

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Ostomy Bag and Its Accessories (H.5900)".

H Gastroenterology-urology devices

H5900 Ostomy bag and accessories

Imported from abroad

Dates and Status

Jun 21, 2019

Jun 21, 2024

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