Taiwan FDA registration cc99c4f0c76ea2b8e6ee7252a76dcaa3
"Bionix" Radiologic Patient Cradle (Non-Sterile)
TW: "畢歐內克" 放射科病患用支架 (未滅菌)
Taiwan·Risk Class 1·MD·BIONIX RADIATION THERAPY·Registered Mar 17, 2015 – Mar 17, 2020CancelledRegistration details
- Analysis ID
- cc99c4f0c76ea2b8e6ee7252a76dcaa3
- License Form
- Ministry of Health Medical Device Import No. 015008
- Customs Code
- DHA09401500807
Company information
- Manufacturer
- BIONIX RADIATION THERAPY
- Manufacturer Country
- United States
- Authorized Representative
- SSGI TAIWAN CO.
Product details
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1830 Stent for radiology patients
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 17, 2015
- Expiry Date
- Mar 17, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "Bionix" Radiologic Patient Cradle (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 cc99c4f0c76ea2b8e6ee7252a76dcaa3 and manufactured by BIONIX RADIATION THERAPY. The authorized representative in Taiwan is SSGI TAIWAN CO..
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