Taiwan FDA registration 04fbf1bcf3dd67816d7be2865352a7bb
“Hybrids” R-Mix Too FreshFrozenCells (Non-sterile)
TW: “海柏” 呼吸道病毒培養細胞 (未滅菌)
Taiwan·Risk Class 1·MD·DIAGNOSTIC HYBRIDS, INC.·Registered Mar 30, 2021 – Mar 30, 2026ExpiredRegistration details
- Analysis ID
- 04fbf1bcf3dd67816d7be2865352a7bb
- License Form
- Ministry of Health Medical Device Import No. 022424
- Customs Code
- DHA09402242402
Company information
- Manufacturer
- DIAGNOSTIC HYBRIDS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GLOWAY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of medical equipment management measures "Cultured animals and human cells (B.2280)".
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B2280 Cultured animal and human cells
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 30, 2021
- Expiry Date
- Mar 30, 2026
About this record
Access comprehensive regulatory information for “Hybrids” R-Mix Too FreshFrozenCells (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 04fbf1bcf3dd67816d7be2865352a7bb and manufactured by DIAGNOSTIC HYBRIDS, INC.. The authorized representative in Taiwan is GLOWAY CO., LTD..
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