Taiwan FDA registration a5d9081baf5d4991dd19090380ceb3ce
"Arkard" ophthalmic ultrasound scanner
TW: “愛可德”眼科超音波掃描儀
Taiwan·Risk Class 2·ACCUTOME, INC.·Registered Sep 30, 2015 – Sep 30, 2020CancelledRegistration details
- Analysis ID
- a5d9081baf5d4991dd19090380ceb3ce
- Customs Code
- DHA05602774409
Company information
- Manufacturer
- ACCUTOME, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BIOMEGA INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1560 Ultrasonic Echo Imaging System;; P.1570 Ultrasonic converters for diagnostic use
- Import Information
- import
Dates and status
- Registration Date
- Sep 30, 2015
- Expiry Date
- Sep 30, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Arkard" ophthalmic 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 a5d9081baf5d4991dd19090380ceb3ce and manufactured by ACCUTOME, INC.. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..
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