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Cell cryogenic equipment for in vitro diagnostics (unsterilized) - Taiwan Registration cd19c67bb83595b1da9fcfd4af744188

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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cd19c67bb83595b1da9fcfd4af744188
Registration Details
Taiwan FDA Registration: cd19c67bb83595b1da9fcfd4af744188
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Device Details

Cell cryogenic equipment for in vitro diagnostics (unsterilized)
TW: "ๆดพ้›ท่ƒฝ" ้ซ”ๅค–่จบๆ–ท็”จ็š„็ดฐ่ƒžๅ†ทๅ‡่จญๅ‚™ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

cd19c67bb83595b1da9fcfd4af744188

DHA04401235507

Company Information

United Kingdom

Product Details

Limited to the first level identification range of cell cryogenic equipment and reactants (B.9225) for in vitro diagnosis of medical device management methods.

B Hematology, pathology, and genetics

B.9225 Cell freezing equipment and reagents for in vitro diagnostics

import

Dates and Status

Nov 09, 2012

Nov 09, 2022

Apr 12, 2024

Cancellation Information

Logged out

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