Taiwan FDA registration 3f316eb7b582e62fea5beb73aa4b0575
Shigella detection reagent and agglutinated serum (unsterilized)
TW: “銳盟”志賀氏桿菌檢測試劑和凝集血清(未滅菌)
Taiwan·Risk Class 1·REMEL EUROPE LIMITED·Registered Apr 04, 2006 – Apr 04, 2026ExpiredRegistration details
- Analysis ID
- 3f316eb7b582e62fea5beb73aa4b0575
- Customs Code
- DHA04400343800
Company information
- Manufacturer
- REMEL EUROPE LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SCN TRADING COMPANY LIMITED
Product details
- Intended Use
- For the detection and identification of Shigella species on solid-state incubators.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3660 志賀氏桿菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Apr 04, 2006
- Expiry Date
- Apr 04, 2026
About this record
Access comprehensive regulatory information for Shigella detection reagent and agglutinated serum (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3f316eb7b582e62fea5beb73aa4b0575 and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.
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