Taiwan FDA registration ebef093ffac235f1bf105c733af2ea61
PADS Manual patient transfer device (Non-sterile)
TW: 沛得適 手動病患輸送裝置 (未滅菌)
Registration details
- Analysis ID
- ebef093ffac235f1bf105c733af2ea61
- License Form
- Ministry of Health Medical Device Import Registration No. a00038
- Customs Code
- DHA084a0003809
Company information
- Manufacturer
- Petermann GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- PADS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Patient Transport Device (J.6785)" 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)
- J6785 Manual Patient Conveyor
Dates and status
- Registration Date
- Jan 10, 2022
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for PADS Manual patient transfer 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 ebef093ffac235f1bf105c733af2ea61 and manufactured by Petermann GmbH. The authorized representative in Taiwan is PADS 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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