Taiwan FDA registration b135ded9c542529531a468c62503fdb0

"Siloam" Mycoplasma Pneumoniae Rapid Test (Non-Sterile)

TW: "西羅亞" 肺炎黴漿菌檢測試劑 (未滅菌)

Taiwan·Risk Class 1·MD·MD BIOTECH CORPORATION·Registered May 23, 2017 – May 23, 2022Expired

Registration details

Analysis ID: b135ded9c542529531a468c62503fdb0
License Form: Ministry of Health Medical Device Import No. 017878
Customs Code: DHA09401787805

Company information

Manufacturer: MD BIOTECH CORPORATION
Manufacturer Country: United States
Authorized Representative: Siloam Biotech Co., Ltd.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological Reagent (C.3375)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C3375 Mycoplasma serum reagent
Import Information: Imported from abroad

Dates and status

Registration Date: May 23, 2017
Expiry Date: May 23, 2022

About this record

Access comprehensive regulatory information for "Siloam" Mycoplasma Pneumoniae Rapid Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b135ded9c542529531a468c62503fdb0 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is Siloam Biotech Co., Ltd..

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