Taiwan FDA registration e0118980ea2d307a7e0681a1d7125c32
“ASTEC” Dry Incubator
TW: “艾司特”乾式培養箱
Taiwan·Risk Class 2·MD·ASTEC CO., LTD.·Registered Aug 13, 2019 – Aug 13, 2024ExpiredRegistration details
- Analysis ID
- e0118980ea2d307a7e0681a1d7125c32
- License Form
- Ministry of Health Medical Device Import No. 032791
- Customs Code
- DHA05603279102
Company information
- Manufacturer
- ASTEC CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- HONG-U SCENTIFIC CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L6120 Assisted reproduction accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 13, 2019
- Expiry Date
- Aug 13, 2024
About this record
Access comprehensive regulatory information for “ASTEC” Dry Incubator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e0118980ea2d307a7e0681a1d7125c32 and manufactured by ASTEC CO., LTD.. The authorized representative in Taiwan is HONG-U SCENTIFIC CORP..
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