Taiwan FDA registration ee724941c1902e4b117269f97f71eb1f
"Prowei" waste collection bag (unsterilized)
TW: “普威”廢液收集袋（未滅菌）
Taiwan·Risk Class 1·Puwei International Co., Ltd. Taishan Factory·Registered Apr 23, 2010 – Apr 23, 2025ExpiredRegistration details
- Analysis ID
- ee724941c1902e4b117269f97f71eb1f
Company information
- Manufacturer
- Puwei International Co., Ltd. Taishan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- UNIMAX MEDICAL SYSTEMS INC.
Product details
- Intended Use
- Limited to the first level of classification and grading management of medical equipment, "Non-powered, single-patient, portable suction equipment (I.4680)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4680 Non-motive, single patient-use, carry-on suctioning device
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 23, 2010
- Expiry Date
- Apr 23, 2025
About this record
Access comprehensive regulatory information for "Prowei" waste collection bag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ee724941c1902e4b117269f97f71eb1f and manufactured by Puwei International Co., Ltd. Taishan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS 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.
Free DatabasePowered by Pure Global AI89,000+ Devices