Taiwan FDA registration 94c4bfe3ebbd73c3c77b9bc08ffbda98
“SYNTEC” Halo System (Non-Sterile)
TW: “亞太”胸頸護架 (未滅菌)
Registration details
- Analysis ID
- 94c4bfe3ebbd73c3c77b9bc08ffbda98
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 001970
- Customs Code
- DHY08300197009
Company information
- Manufacturer
- SYNTEC SCIENTIFIC CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SYNTEC SCIENTIFIC CORPORATION
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3490 Torso Gear
- Import Information
- Produced in Taiwan, China
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 “SYNTEC” Halo System (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 94c4bfe3ebbd73c3c77b9bc08ffbda98 and manufactured by SYNTEC SCIENTIFIC CORPORATION. The authorized representative in Taiwan is SYNTEC SCIENTIFIC CORPORATION.
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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