Taiwan FDA registration ef49fb6c383f13bc5cf26d6a6c2d62d2
Omega-rapid latex agglutination reagent-streptococcal group
TW: 奧米加-快速乳膠凝集試劑-鏈球菌群
Registration details
- Analysis ID
- ef49fb6c383f13bc5cf26d6a6c2d62d2
- Customs Code
- DHA04400548605
Company information
- Manufacturer
- OMEGA DIAGNOSTICS LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EUGENE-CHEN CO., LTD.
Product details
- Intended Use
- Restriction of medical device management methods Streptococcus belongs to the first level identification range of serum reagent (C.3740).
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3740 鏈球菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Dec 29, 2006
- Expiry Date
- Dec 29, 2011
- Cancellation Date
- Oct 29, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Omega-rapid latex agglutination reagent-streptococcal group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ef49fb6c383f13bc5cf26d6a6c2d62d2 and manufactured by OMEGA DIAGNOSTICS LTD.. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..
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