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"HandyRehab" Continuous Passive Motion Device (Non-sterile) - Taiwan Registration ddb220d1bc3f02384971becc7a30c175

Access comprehensive regulatory information for "HandyRehab" 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 ddb220d1bc3f02384971becc7a30c175 and manufactured by ZUNOSAKI LIMITED.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS 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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ddb220d1bc3f02384971becc7a30c175
Registration Details
Taiwan FDA Registration: ddb220d1bc3f02384971becc7a30c175
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Device Details

"HandyRehab" Continuous Passive Motion Device (Non-sterile)
TW: "้Ÿ“่ฟช็‘ž่ณ€ๅš" ้€ฃ็บŒๅผ่ขซๅ‹•้—œ็ฏ€ๆดปๅ‹•ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ddb220d1bc3f02384971becc7a30c175

Ministry of Health Medical Device Import No. 022276

DHA09402227600

Company Information

Hong Kong

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Continuous Passive Joint Activator (O.0006)".

o Equipment for physical medicine

O0006 Continuous Passive Joint Activator

Imported from abroad

Dates and Status

Jan 28, 2021

Jan 28, 2026