Taiwan FDA registration 417355d55d30706e8944891de5acca0b
"TECHNIX" Radiographic intensifying screen (Non-Sterile)
TW: "塔克尼克" 放射線強化螢幕 (未滅菌)
Registration details
- Analysis ID
- 417355d55d30706e8944891de5acca0b
- License Form
- Ministry of Health Medical Device Import No. 016521
- Customs Code
- DHA09401652101
Company information
- Manufacturer
- TECHNIX S. P. A.
- Manufacturer Country
- Italy
- Authorized Representative
- SERVICETECH INTERNATIONAL INC.
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Radiation Enhanced Screen (P.1960)".
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1960 Radiation Enhancement Screen
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 12, 2016
- Expiry Date
- May 12, 2026
About this record
Access comprehensive regulatory information for "TECHNIX" Radiographic intensifying screen (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 417355d55d30706e8944891de5acca0b and manufactured by TECHNIX S. P. A.. The authorized representative in Taiwan is SERVICETECH INTERNATIONAL INC..
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