Taiwan FDA registration bf219a9fee18ac58b113000a1c47a68d
“Strengthen” Protective Restraint (Non-Sterile)
TW: “強生”保護性限制帶 (未滅菌)
Registration details
- Analysis ID
- bf219a9fee18ac58b113000a1c47a68d
- License Form
- Ministry of Health Medical Device Import No. 013530
- Customs Code
- DHA09401353000
Company information
- Manufacturer
- ALLIANCE MANUFACTURING SERVICE, INC.
- Manufacturer Country
- Hong Kong
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6760 Protective Restraint Band
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 24, 2013
- Expiry Date
- Oct 24, 2018
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Strengthen” Protective Restraint (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 bf219a9fee18ac58b113000a1c47a68d 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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