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"SKYLOTEC" ultraRoll STRETCHER (Non-sterile) - Taiwan Registration 56961690fbd12b1c249285d962cda51f

Access comprehensive regulatory information for "SKYLOTEC" ultraRoll STRETCHER (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 56961690fbd12b1c249285d962cda51f and manufactured by SKYLOTEC GmbH. The authorized representative in Taiwan is TODAY'S 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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56961690fbd12b1c249285d962cda51f
Registration Details
Taiwan FDA Registration: 56961690fbd12b1c249285d962cda51f
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Device Details

"SKYLOTEC" ultraRoll STRETCHER (Non-sterile)
TW: "ๆ–ฏๆณฐ้พๆณฐๅ…‹"ๅฅง็‰น ๆ‰‹ๆๅผๆ“”ๆžถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

56961690fbd12b1c249285d962cda51f

Ministry of Health Medical Device Import Registration No. a00103

DHA084a0010307

Company Information

Germany

Product Details

Limited to the first level identification scope of the "portable stretcher (J.6900)" of the Measures for the Classification and Grading Management of Medical Equipment.

J General hospital and personal use equipment

J6900 portable stretcher

Dates and Status

Aug 30, 2022

Oct 31, 2023