Taiwan FDA registration 13f8c334cf86001492f392d48a731cce
"Bintri" torso device (unsterilized)
TW: "賓特立" 軀幹裝具 (未滅菌)
Registration details
- Analysis ID
- 13f8c334cf86001492f392d48a731cce
Company information
- Manufacturer
- PINTOLI ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PINTOLI ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "Torso Equipment (O.3490)" classification and grading management measures for medical equipment.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3490 Torso mounting
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Bintri" torso device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 13f8c334cf86001492f392d48a731cce and manufactured by PINTOLI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is PINTOLI ENTERPRISE CO., LTD..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices