Taiwan FDA registration fb6287276020ebcd877e7eaa87ee123d
“BIONET” Mobile Ultrasound Scanner
TW: “百歐能” 攜帶型超音波掃描儀
Taiwan·Risk Class 2·MD·Bionet Co., Ltd.·Registered Dec 02, 2014 – Dec 02, 2019CancelledRegistration details
- Analysis ID
- fb6287276020ebcd877e7eaa87ee123d
- License Form
- Ministry of Health Medical Device Import No. 026692
- Customs Code
- DHA05602669201
Company information
- Manufacturer
- Bionet Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- K2 INTERNATIONAL MEDICAL INC.
Product details
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1560 ultrasonic echo imaging system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 02, 2014
- Expiry Date
- Dec 02, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for “BIONET” Mobile Ultrasound Scanner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb6287276020ebcd877e7eaa87ee123d and manufactured by Bionet Co., Ltd.. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices