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Yihinda pneumoniae antibody reagent (unsterilized) - Taiwan Registration 09aa56054a5640e8fa56085486bb7bb9

Access comprehensive regulatory information for Yihinda pneumoniae antibody reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 09aa56054a5640e8fa56085486bb7bb9 and manufactured by WEIFANG KANGHUA BIOTECH CO., LTD. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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09aa56054a5640e8fa56085486bb7bb9
Registration Details
Taiwan FDA Registration: 09aa56054a5640e8fa56085486bb7bb9
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Device Details

Yihinda pneumoniae antibody reagent (unsterilized)
TW: ๆฏ…ๆฌฃ้”่‚บ็‚Ž้ฐดๆผฟ่ŒๆŠ—้ซ”่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

09aa56054a5640e8fa56085486bb7bb9

DHA04600119302

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological Reagent (C.3375)".

C Immunology and microbiology

C.3375 ้ปดๆผฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

Chinese goods;; input

Dates and Status

Dec 14, 2010

Dec 14, 2020

Jun 07, 2022

Cancellation Information

Logged out

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