Taiwan FDA registration a2418a5a9fa356672630dd487ea390e2

Spectac Minimally Invasive Brain Surgery System (Sterilization)

TW: 視博腦微創手術系統(滅菌)

Taiwan·Risk Class 2·Baili Medical Products Co., Ltd.;; Kunyu Technology Co., Ltd·Registered Oct 09, 2024 – Oct 09, 2029Active

Registration details

Analysis ID: a2418a5a9fa356672630dd487ea390e2

Company information

Manufacturer: Baili Medical Products Co., Ltd.;; Kunyu Technology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SYNERGY BIOMEDICAL LTD.

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4800 神經外科用自留牽開器
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Oct 09, 2024
Expiry Date: Oct 09, 2029

About this record

Access comprehensive regulatory information for Spectac Minimally Invasive Brain Surgery System (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a2418a5a9fa356672630dd487ea390e2 and manufactured by Baili Medical Products Co., Ltd.;; Kunyu Technology Co., Ltd. The authorized representative in Taiwan is SYNERGY BIOMEDICAL LTD..

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