Taiwan FDA registration 1fbb01fa4086ce61fb08f30f82931bb6
Axis-Shield MICROSYPH TPHA
TW: 艾克西斯梅毒螺旋體血球凝集試劑
Taiwan·Risk Class 2·MD·AXIS-SHIELD DIAGNOSTICS LTD.·Registered Dec 08, 2016 – Dec 08, 2021CancelledRegistration details
- Analysis ID
- 1fbb01fa4086ce61fb08f30f82931bb6
- License Form
- Ministry of Health Medical Device Import No. 029159
- Customs Code
- DHA05602915908
Company information
- Manufacturer
- AXIS-SHIELD DIAGNOSTICS LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- HONEST MEDICAL INC.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3830 Treponema pallidum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 08, 2016
- Expiry Date
- Dec 08, 2021
- Cancellation Date
- Aug 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Axis-Shield MICROSYPH TPHA in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fbb01fa4086ce61fb08f30f82931bb6 and manufactured by AXIS-SHIELD DIAGNOSTICS LTD.. The authorized representative in Taiwan is HONEST MEDICAL INC..
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