Taiwan FDA registration 487bc262f970a09d0037f2ac48030305
"Changgu" anesthesia breathing line and its spare parts (unsterilized)
TW: "長固"麻醉呼吸管路及其零配件(未滅菌)
Registration details
- Analysis ID
- 487bc262f970a09d0037f2ac48030305
- Customs Code
- DHY04300117901
Company information
- Manufacturer
- PHOENIX INSTRUMENT BUSINESS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PHOENIX INSTRUMENT BUSINESS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management measures for medical equipment "anesthesia breathing circuit (D.5240)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5240 麻醉呼吸管路
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 07, 2006
- Expiry Date
- Apr 07, 2026
About this record
Access comprehensive regulatory information for "Changgu" anesthesia breathing line and its spare parts (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 487bc262f970a09d0037f2ac48030305 and manufactured by PHOENIX INSTRUMENT BUSINESS CO., LTD.. The authorized representative in Taiwan is PHOENIX INSTRUMENT BUSINESS 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