Taiwan FDA registration 582150c231a336d95a36eaed2fba0ea5
"Promega" digital 3D X-ray imaging system
TW: “普洛美嘉”數位三維X光影像系統
Taiwan·Risk Class 2·PLANMECA LTD·Registered Nov 12, 2019 – Nov 12, 2029ActiveRegistration details
- Analysis ID
- 582150c231a336d95a36eaed2fba0ea5
- Customs Code
- DHAS5603299306
Company information
- Manufacturer
- PLANMECA LTD
- Manufacturer Country
- Finland
- Authorized Representative
- MIDEAL TECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.1800 口腔外X光照射系統
- Import Information
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
- Registration Date
- Nov 12, 2019
- Expiry Date
- Nov 12, 2029
About this record
Access comprehensive regulatory information for "Promega" digital 3D X-ray imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 582150c231a336d95a36eaed2fba0ea5 and manufactured by PLANMECA LTD. The authorized representative in Taiwan is MIDEAL TECHNOLOGY CO., LTD..
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