Taiwan FDA registration 9d5893c316114d9d8f6e1115c16bec7b

"Menaris" chemical cold light allergen automatic analyzer

TW: “梅納麗斯”化學冷光過敏原自動分析儀
Taiwan flagTaiwan·Risk Class 2·MINARIS MEDICAL AMERICA, INC.·Registered May 08, 2006 – May 08, 2026Expired
Registration details
Analysis ID
9d5893c316114d9d8f6e1115c16bec7b
Customs Code
DHA00601656403
Company information
Manufacturer Country
United States
Authorized Representative
MED PHAR ENTERPRISE CO., LTD.
Product details
Intended Use
Can be used to test for specific allergenic reactions to multiple items simultaneously.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.5750 Radioallergen adsorption immunoassay system
Import Information
import
Dates and status
Registration Date
May 08, 2006
Expiry Date
May 08, 2026
About this record

Access comprehensive regulatory information for "Menaris" chemical cold light allergen automatic analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9d5893c316114d9d8f6e1115c16bec7b and manufactured by MINARIS MEDICAL AMERICA, INC.. The authorized representative in Taiwan is MED PHAR ENTERPRISE 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