Taiwan FDA registration f4ad5e0a92192e73d1371accd2759f13
Bio-Rad IH-QC Modular System
TW: 伯瑞血庫品管模組系統
Registration details
- Analysis ID
- f4ad5e0a92192e73d1371accd2759f13
- License Form
- Ministry of Health Medical Device Import No. 030546
- Customs Code
- DHA05603054602
Company information
- Manufacturer
- DIAMED GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
Product details
- Intended Use
- This product is used for quality management of ID-Cassette systems using manual and/or instrumental determination of ABO systems, Rh(RH) systems, Kell (KEL) systems, and/or further immunohematology tests.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9650 Quality control equipment for blood bank reactors
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 23, 2018
- Expiry Date
- Apr 23, 2028
About this record
Access comprehensive regulatory information for Bio-Rad IH-QC Modular System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f4ad5e0a92192e73d1371accd2759f13 and manufactured by DIAMED GMBH. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
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.
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