Taiwan FDA registration 56dd964d9903939f74cd6e89865946dd

Inorganic phosphorus reagent set (unsterilized)

TW: 〝朕江〞無機磷試劑套組 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·LANNER BIOTECHNOLOGY CO., LTD.·Registered Nov 21, 2011 – Nov 21, 2021Cancelled
Registration details
Analysis ID
56dd964d9903939f74cd6e89865946dd
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
LANNER BIOTECHNOLOGY CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Phosphorous Acid (Inorganic) Test System (A.1580)".
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1580 Phosphoric acid (inorganic) test system
Import Information
Domestic
Dates and status
Registration Date
Nov 21, 2011
Expiry Date
Nov 21, 2021
Cancellation Date
Dec 11, 2023
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 Inorganic phosphorus reagent set (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 56dd964d9903939f74cd6e89865946dd and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LANNER BIOTECHNOLOGY CO., LTD., 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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