Taiwan FDA registration 950ecc6543e2dae4f50b316b460d8c87
"Schweis" Veterans Pneumonia Urine Antigen Test Reagent (Unsterilized)
TW: "史威斯" 退伍軍人肺炎尿液抗原檢測試劑(未滅菌)
Registration details
- Analysis ID
- 950ecc6543e2dae4f50b316b460d8c87
- Customs Code
- DHA04401129602
Company information
- Manufacturer
- SA SCIENTIFIC INC.
- Manufacturer Country
- United States
- Authorized Representative
- RAFA INTERNATIONAL CORP.
Product details
- Intended Use
- Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3300 嗜血桿菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Jan 13, 2012
- Expiry Date
- Jan 13, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Schweis" Veterans Pneumonia Urine Antigen Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 950ecc6543e2dae4f50b316b460d8c87 and manufactured by SA SCIENTIFIC INC.. The authorized representative in Taiwan is RAFA INTERNATIONAL CORP..
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