Taiwan FDA registration da6fdf059b39701f5330a6ce3fa0250d
"Novatec" NovaLisa Coxiella burnetii (Q-Fever) Phase 2 IgM (Non-Sterile)
TW: "諾瓦德" 諾瓦莉莎Q熱第二階段IgM酵素免疫試驗組 (未滅菌)
Taiwan·Risk Class 1·MD·NOVATEC IMMUNDIAGNOSTICA GMBH·Registered Dec 02, 2015 – Dec 02, 2020CancelledRegistration details
- Analysis ID
- da6fdf059b39701f5330a6ce3fa0250d
- License Form
- Ministry of Health Medical Device Import No. 015916
- Customs Code
- DHA09401591603
Company information
- Manufacturer
- NOVATEC IMMUNDIAGNOSTICA GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- STANDARD MOLECULES INC.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3500 rickettsial serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 02, 2015
- Expiry Date
- Dec 02, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "Novatec" NovaLisa Coxiella burnetii (Q-Fever) Phase 2 IgM (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 da6fdf059b39701f5330a6ce3fa0250d and manufactured by NOVATEC IMMUNDIAGNOSTICA GMBH. The authorized representative in Taiwan is STANDARD MOLECULES 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