Taiwan FDA registration bcced25095a452beba9362dd90455e68
"TAITUNG" Infusion stand (Non-Sterile)
TW: "台同"點滴架(未滅菌)
Registration details
- Analysis ID
- bcced25095a452beba9362dd90455e68
- License Form
- Ministry of Health Medical Device Manufacturing No. 008203
Company information
- Manufacturer
- Taitong Instrument Co., Ltd. Tainan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Taitong Instrument Co., Ltd. Tainan Factory
Product details
- Intended Use
- Limited to the first level identification range of the "Injection Rack (J.6990)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6990 Injection rack
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 21, 2020
- Expiry Date
- Feb 21, 2025
About this record
Access comprehensive regulatory information for "TAITUNG" Infusion stand (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 bcced25095a452beba9362dd90455e68 and manufactured by Taitong Instrument Co., Ltd. Tainan Factory. The authorized representative in Taiwan is Taitong Instrument Co., Ltd. Tainan Factory.
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