Taiwan FDA registration a1839e7c9074adf85243a89e3f7b550f
“Neodyne”Silicone Scar-care Dressing (Non-Sterile)
TW: “尼德”疤痕護理矽膠片 (未滅菌)
Registration details
- Analysis ID
- a1839e7c9074adf85243a89e3f7b550f
- License Form
- Ministry of Health Medical Device Import No. 013735
- Customs Code
- DHA09401373502
Company information
- Manufacturer
- NEODYNE BIOSCIENCES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Robbie Jenny International Inc
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4025 silicone sheet
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 27, 2013
- Expiry Date
- Dec 27, 2018
- Cancellation Date
- Feb 11, 2019
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for “Neodyne”Silicone Scar-care Dressing (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 a1839e7c9074adf85243a89e3f7b550f and manufactured by NEODYNE BIOSCIENCES, INC.. The authorized representative in Taiwan is Robbie Jenny International 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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