Taiwan FDA registration cd19c67bb83595b1da9fcfd4af744188

Cell cryogenic equipment for in vitro diagnostics (unsterilized)

TW: "派雷能" 體外診斷用的細胞冷凍設備 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·PLANNER PLC·Registered Nov 09, 2012 – Nov 09, 2022Cancelled
Registration details
Analysis ID
cd19c67bb83595b1da9fcfd4af744188
Customs Code
DHA04401235507
Company information
Manufacturer
PLANNER PLC
Manufacturer Country
United Kingdom
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
Nov 09, 2012
Expiry Date
Nov 09, 2022
Cancellation Date
Apr 12, 2024
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 cryogenic equipment 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 cd19c67bb83595b1da9fcfd4af744188 and manufactured by PLANNER PLC. The authorized representative in Taiwan is LabIVF Taiwan International Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including IC Biomedical, Niostria Co., Ltd. Biomedical Factory, and 2 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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