Taiwan FDA registration 9c2c5513d714532b4f4be808533c69ef
“Strengthen”Manual patient transfer device (Non-Sterile)
TW: “強生”手動病患輸送裝置 (未滅菌)
Taiwan·Risk Class 1·MD·ALLIANCE MANUFACTURING SERVICE, INC.·Registered Oct 01, 2021 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- 9c2c5513d714532b4f4be808533c69ef
- License Form
- Ministry of Health Medical Device Import Registration No. 012202
- Customs Code
- DHA08401220205
Company information
- Manufacturer
- ALLIANCE MANUFACTURING SERVICE, INC.
- Manufacturer Country
- Hong Kong
- Authorized Representative
- Johnson & Johnson Medical Devices, Inc
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6785 Manual Patient Conveyor
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for “Strengthen”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 9c2c5513d714532b4f4be808533c69ef and manufactured by ALLIANCE MANUFACTURING SERVICE, INC.. The authorized representative in Taiwan is Johnson & Johnson Medical Devices, Inc.
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