Taiwan FDA registration b00c9b420a61df4341a9caebde6c4e5b
"GOKO" Liquid crystal vein locator (Non-Sterile)
TW: "構蔻" 液晶靜脈定位器 (未滅菌)
Registration details
- Analysis ID
- b00c9b420a61df4341a9caebde6c4e5b
- License Form
- Ministry of Health Medical Device Import No. 020480
- Customs Code
- DHA09402048002
Company information
- Manufacturer
- GOKO IMAGING DEVICES CO., LTD
- Manufacturer Country
- Japan
- Authorized Representative
- TRUGENE DIAGNOSTICS, INC.
Product details
- Intended Use
- Limited to the first level identification range of the "liquid crystal vein locator (J.6970)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6970 LCD Vein Locator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 24, 2019
- Expiry Date
- May 24, 2024
About this record
Access comprehensive regulatory information for "GOKO" Liquid crystal vein locator (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 b00c9b420a61df4341a9caebde6c4e5b and manufactured by GOKO IMAGING DEVICES CO., LTD. The authorized representative in Taiwan is TRUGENE DIAGNOSTICS, INC..
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