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"HandiMove" Non-AC-powered patient lift (Non-sterile) - Taiwan Registration ce4002924d084f7d479df9ad4d770ff8

Access comprehensive regulatory information for "HandiMove" Non-AC-powered patient lift (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 ce4002924d084f7d479df9ad4d770ff8 and manufactured by HANDI-MOVE INTERNATIONAL. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.

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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ce4002924d084f7d479df9ad4d770ff8
Registration Details
Taiwan FDA Registration: ce4002924d084f7d479df9ad4d770ff8
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Device Details

"HandiMove" Non-AC-powered patient lift (Non-sterile)
TW: "ๆผขๅœฐ้ญ”่ผ”" ้žไบคๆต้›ปๅŠ›ๅผ็—…ๆ‚ฃๅ‡้™ๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ce4002924d084f7d479df9ad4d770ff8

Ministry of Health Medical Device Import No. 017176

DHA09401717602

Company Information

Belgium

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".

J General hospital and personal use equipment

J5510 Non-AC Electric Patient Lift

Imported from abroad

Dates and Status

Nov 15, 2016

Nov 15, 2021