Taiwan FDA registration 60307e0b94e8a75384034031cb3def25
“KUBTEC” Digital Specimen Radiography System
TW: “柯博特” 組織樣本數位化影像系統
Taiwan·Risk Class 2·MD·KUB Technologies Inc.·Registered Sep 17, 2021 – Sep 17, 2026ActiveRegistration details
- Analysis ID
- 60307e0b94e8a75384034031cb3def25
- License Form
- Ministry of Health Medical Device Import No. 034863
- Customs Code
- DHA05603486308
Company information
- Manufacturer
- KUB Technologies Inc.
- Manufacturer Country
- United States
- Authorized Representative
- PROMEDICS TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1680 stationary X-ray system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 17, 2021
- Expiry Date
- Sep 17, 2026
About this record
Access comprehensive regulatory information for “KUBTEC” Digital Specimen Radiography System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60307e0b94e8a75384034031cb3def25 and manufactured by KUB Technologies Inc.. The authorized representative in Taiwan is PROMEDICS TECHNOLOGY CO., LTD..
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