Taiwan FDA registration 30f510157ad47f10e4577179de14a710

Cell freezing equipment and reactants for in vitro diagnosis (unsterilized)

TW: “磊柏”體外診斷用的細胞冷凍設備及反應劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·CRYOTECH CO., LTD.·Registered Apr 26, 2013 – Apr 26, 2023Expired
Registration details
Analysis ID
30f510157ad47f10e4577179de14a710
Customs Code
DHA04401294604
Company information
Manufacturer
CRYOTECH CO., LTD.
Manufacturer Country
Japan
Authorized Representative
LabIVF Taiwan International Co., Ltd
Product details
Intended Use
Limited to the first level identification range of cell cryogenic equipment and reactants (B.9225) for in vitro diagnosis of medical device management methods.
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
import
Dates and status
Registration Date
Apr 26, 2013
Expiry Date
Apr 26, 2023
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About this record

Access comprehensive regulatory information for Cell freezing equipment and reactants for in vitro diagnosis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 30f510157ad47f10e4577179de14a710 and manufactured by CRYOTECH CO., LTD.. The authorized representative in Taiwan is LabIVF Taiwan International Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including METRIGEN, and 1 recent registrations in the same category. 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.

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