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"Romedick" patient lift (unsterilized) - Taiwan Registration 443b22f0246e2f79ba859137da4f7619

Access comprehensive regulatory information for "Romedick" patient lift (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 443b22f0246e2f79ba859137da4f7619 and manufactured by ROMEDIC AB. The authorized representative in Taiwan is THERALIFE INTERVENTION CARE COMPANY LIMITED.

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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443b22f0246e2f79ba859137da4f7619
Registration Details
Taiwan FDA Registration: 443b22f0246e2f79ba859137da4f7619
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Device Details

"Romedick" patient lift (unsterilized)
TW: โ€œ็พ…้บฅ่ฟชๅ…‹โ€็—…ๆ‚ฃ็งปไฝๅ‡้™ๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

443b22f0246e2f79ba859137da4f7619

DHA04400828701

Company Information

Sweden

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

J.5510 Non-AC electric patient lifts

Domestic

Dates and Status

Nov 10, 2009

Nov 10, 2019

Jun 16, 2022

Cancellation Information

Logged out

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