Taiwan FDA registration d3d386a12d8245f77acd1e9463560ec0
“Strengthen” Immobile Brace (Non-sterile)
TW: “強生”固定式護具（未滅菌）
Taiwan·Risk Class 1·MD·ALLIANCE MANUFACTURING SERVICE, INC.·Registered Oct 01, 2021 – Oct 31, 2022CancelledRegistration details
- Analysis ID
- d3d386a12d8245f77acd1e9463560ec0
- License Form
- Ministry of Health Medical Device Import Registration No. 012203
- Customs Code
- DHA08401220307
Company information
- Manufacturer
- ALLIANCE MANUFACTURING SERVICE, INC.
- Manufacturer Country
- Hong Kong
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Strengthen” Immobile Brace (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 d3d386a12d8245f77acd1e9463560ec0 and manufactured by ALLIANCE MANUFACTURING SERVICE, INC.. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.
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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