Taiwan FDA registration 56961690fbd12b1c249285d962cda51f
"SKYLOTEC" ultraRoll STRETCHER (Non-sterile)
TW: "斯泰龍泰克"奧特 手提式擔架 (未滅菌)
Registration details
- Analysis ID
- 56961690fbd12b1c249285d962cda51f
- License Form
- Ministry of Health Medical Device Import Registration No. a00103
- Customs Code
- DHA084a0010307
Company information
- Manufacturer
- SKYLOTEC GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- TODAY'S INSTRUMENTS CO., LTD.
Product details
- Intended Use
- 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.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6900 portable stretcher
Dates and status
- Registration Date
- Aug 30, 2022
- Expiry Date
- Oct 31, 2023
About this record
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..
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