Taiwan FDA registration aa5859d54f3dd3455a47695cfaaa8ad2
Protect your body 16/18 human papillomavirus DNA DNA test kit
TW: 護妳身16/18型人類乳突病毒去氧核醣核酸檢測套組
Taiwan·Risk Class 3·HOLOGIC, INC.·Registered Jun 03, 2013 – Jun 03, 2018CancelledRegistration details
- Analysis ID
- aa5859d54f3dd3455a47695cfaaa8ad2
- Customs Code
- DHA00602471000
Company information
- Manufacturer
- HOLOGIC, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BIO-CHECK LABORATORIES LTD.
Product details
- Intended Use
- The Cervista 16/18 Human Papillomavirus (HPV) DNA Panel is an in vitro diagnostic test for the qualitative detection of human papillomavirus (HPV) DNA types 16 and 18 in cervical samples.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.0004 Human papillomavirus serum reagent
- Import Information
- import
Dates and status
- Registration Date
- Jun 03, 2013
- Expiry Date
- Jun 03, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Protect your body 16/18 human papillomavirus DNA DNA test kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number aa5859d54f3dd3455a47695cfaaa8ad2 and manufactured by HOLOGIC, INC.. The authorized representative in Taiwan is BIO-CHECK LABORATORIES 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