Taiwan FDA registration d679026575b530bcb7808a5eda4f47d9

Shinohara zinc test system

TW: 筱原鋅試驗系統
Taiwan flagTaiwan·Risk Class 2·SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER·Registered Nov 12, 2010 – Nov 12, 2020Cancelled
Registration details
Analysis ID
d679026575b530bcb7808a5eda4f47d9
Customs Code
DHA00602180200
Company information
Manufacturer Country
Japan
Authorized Representative
MEDICARE PRODUCTS INC.
Product details
Intended Use
Suitable for use with Hitachi automated analyzers to measure zinc (Zn) levels in serum and plasma.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Import Information
import
Dates and status
Registration Date
Nov 12, 2010
Expiry Date
Nov 12, 2020
Cancellation Date
Jun 22, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for Shinohara zinc test system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d679026575b530bcb7808a5eda4f47d9 and manufactured by SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..

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