Taiwan FDA registration d679026575b530bcb7808a5eda4f47d9
Shinohara zinc test system
TW: 筱原鋅試驗系統
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