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"FURNISS" Continuous Passive Motion Device (Non-Sterile) - Taiwan Registration fbd86d16141ca2f4937417537991ea88

Access comprehensive regulatory information for "FURNISS" Continuous Passive Motion Device (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 fbd86d16141ca2f4937417537991ea88 and manufactured by The Furniss Corporation Ltd.. The authorized representative in Taiwan is PROMEDICAL 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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fbd86d16141ca2f4937417537991ea88
Registration Details
Taiwan FDA Registration: fbd86d16141ca2f4937417537991ea88
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Device Details

"FURNISS" Continuous Passive Motion Device (Non-Sterile)
TW: "่Šฌๅฐผๆ–ฏ" ้€ฃ็บŒๅผ่ขซๅ‹•้—œ็ฏ€ๆดปๅ‹•ๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

fbd86d16141ca2f4937417537991ea88

Ministry of Health Medical Device Import No. 022970

DHA09402297000

Company Information

United States

Product Details

Limited to the first level identification range of the classification and grading management method for medical equipment "Continuous Passive Joint Activator (O.0006)".

o Physical Medical Sciences

O0006 Continuous Passive Joint Activator

Imported from abroad

Dates and Status

Dec 01, 2022

Dec 01, 2027