Taiwan FDA registration ae7f50458f25a4bf297bfd0047f2bc74
"Keina" aseptic needle needle
TW: "慶名" 無菌針灸針
Registration details
- Analysis ID
- ae7f50458f25a4bf297bfd0047f2bc74
- Customs Code
- DHY00500120301
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Qingming Medical Equipment Co., Ltd. Wugu Factory
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Import Information
- Domestic
Dates and status
- Registration Date
- Nov 24, 2004
- Expiry Date
- Nov 24, 2029
About this record
Access comprehensive regulatory information for "Keina" aseptic needle needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae7f50458f25a4bf297bfd0047f2bc74 and manufactured by Qingming Medical Equipment Co., Ltd. Wugu Factory. The authorized representative in Taiwan is Qingming Medical Equipment Co., Ltd. Wugu 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