Taiwan FDA registration 98875864f79d124c558f5366b3c03161

Cell cryonics equipment and reactants for in vitro diagnostics

TW: “/眽S亞瑟克”體外診斷用的細胞冷凍設備及反應劑
Taiwan flagTaiwan·Risk Class 1·ZELTIQ AESTHETICS, INC.·Registered Nov 12, 2010 – Nov 12, 2015Cancelled
Registration details
Analysis ID
98875864f79d124c558f5366b3c03161
Customs Code
DHA04400950200
Company information
Manufacturer Country
United States
Authorized Representative
Conservation Corporation Limited
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
Nov 12, 2010
Expiry Date
Nov 12, 2015
Cancellation Date
Jun 25, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for Cell cryonics equipment and reactants for in vitro diagnostics in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 98875864f79d124c558f5366b3c03161 and manufactured by ZELTIQ AESTHETICS, INC.. The authorized representative in Taiwan is Conservation Corporation Limited.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including PROMOITALIA GROUP S.P.A, PLANER Limited, and 4 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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