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Inorganic phosphorus reagent set (unsterilized) - Taiwan Registration 56dd964d9903939f74cd6e89865946dd

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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56dd964d9903939f74cd6e89865946dd
Registration Details
Taiwan FDA Registration: 56dd964d9903939f74cd6e89865946dd
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Device Details

Inorganic phosphorus reagent set (unsterilized)
TW: ใ€ๆœ•ๆฑŸใ€ž็„กๆฉŸ็ฃท่ฉฆๅŠ‘ๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

56dd964d9903939f74cd6e89865946dd

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Phosphorous Acid (Inorganic) Test System (A.1580)".

A Clinical chemistry and clinical toxicology

A.1580 Phosphoric acid (inorganic) test system

Domestic

Dates and Status

Nov 21, 2011

Nov 21, 2021

Dec 11, 2023

Cancellation Information

Logged out

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