Taiwan FDA registration ffd2904043eede2b2e16a1fdaf177890
“Hologic” Urine Specimen Collection Kit (Non-sterile)
TW: “豪洛捷”尿液檢體收集及運送套組 (未滅菌)
Taiwan·Risk Class 1·MD·HOLOGIC, INC.·Registered Feb 21, 2014 – Feb 21, 2024ExpiredRegistration details
- Analysis ID
- ffd2904043eede2b2e16a1fdaf177890
- License Form
- Ministry of Health Medical Device Import No. 013866
- Customs Code
- DHA09401386604
Company information
- Manufacturer
- HOLOGIC, INC.
- Manufacturer Country
- United States
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Sample Collection and Delivery Equipment (C.2900)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2900 Microbial sample collection and delivery device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 21, 2014
- Expiry Date
- Feb 21, 2024
About this record
Access comprehensive regulatory information for “Hologic” Urine Specimen Collection Kit (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 ffd2904043eede2b2e16a1fdaf177890 and manufactured by HOLOGIC, INC.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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