Taiwan FDA registration 18f12a24bb57cd94bdd5d903d4db4e85
Reagent for Mitsubishi urine microalbumin determination
TW: 三菱尿微量白蛋白測定用試劑
Registration details
- Analysis ID
- 18f12a24bb57cd94bdd5d903d4db4e85
- Customs Code
- DHA00601719200
Company information
- Manufacturer
- MITSUBISHI KAGAKU IATRON. INC.
- Manufacturer Country
- Japan
- Authorized Representative
- Jingxiang Co., Ltd
Product details
- Intended Use
- The amount of albumin in the urine is measured.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1035 Albumin Testing System
- Import Information
- import
Dates and status
- Registration Date
- Jul 04, 2006
- Expiry Date
- Jul 04, 2011
- Cancellation Date
- May 23, 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 urine microalbumin determination in Taiwan's medical device market through Pure Global AI's free database. is registered under number 18f12a24bb57cd94bdd5d903d4db4e85 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