Taiwan FDA registration ed1f24cab9258947e5cc0feddceb9093
"HOHAN" cell cryogenic equipment and reactants for in vitro diagnostics (unsterilized)
TW: "浩翰" 體外診斷用的細胞冷凍設備及反應劑 (未滅菌)
Registration details
- Analysis ID
- ed1f24cab9258947e5cc0feddceb9093
- Customs Code
- DHA09600450602
Company information
- Manufacturer
- DANCLAN BIO TECH CHENGDU CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- LABCHINA (TAIWAN) CO., LIMITED
Product details
- Intended Use
- Limited to the classification and grading management of medical devices, "Cell cryonics equipment and reactants for in vitro diagnosis (B.9225)" Grade 1 identification range.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9225 Cell freezing equipment and reagents for in vitro diagnostics
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Apr 26, 2021
- Expiry Date
- Apr 26, 2026
About this record
Access comprehensive regulatory information for "HOHAN" cell cryogenic equipment and reactants for in vitro diagnostics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ed1f24cab9258947e5cc0feddceb9093 and manufactured by DANCLAN BIO TECH CHENGDU CO., LTD. The authorized representative in Taiwan is LABCHINA (TAIWAN) CO., LIMITED.
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