Taiwan FDA registration e7f2e489ca19ca4a4431f688118aa413
Reagent for Mitsubishi immunoglobulin M assay
TW: 三菱免疫球蛋白M測定用試劑
Taiwan·Risk Class 2·MITSUBISHI KAGAKU IATRON. INC.·Registered Jul 05, 2006 – Jul 05, 2011CancelledRegistration details
- Analysis ID
- e7f2e489ca19ca4a4431f688118aa413
- Customs Code
- DHA00601719503
Company information
- Manufacturer
- MITSUBISHI KAGAKU IATRON. INC.
- Manufacturer Country
- Japan
- Authorized Representative
- Jingxiang Co., Ltd
Product details
- Intended Use
- The haze of immunoglobulin M (IgM) in serum was analyzed.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5510 免疫球蛋白A,G,M,D及E免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Jul 05, 2006
- Expiry Date
- Jul 05, 2011
- Cancellation Date
- Oct 30, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Reagent for Mitsubishi immunoglobulin M assay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e7f2e489ca19ca4a4431f688118aa413 and manufactured by MITSUBISHI KAGAKU IATRON. INC.. The authorized representative in Taiwan is Jingxiang Co., Ltd.
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