Taiwan FDA registration 293b81036d39aff8a5893d5e939fba05
"Medspira" Radiologic patient cradle (Non-Sterile)
TW: "美德斯" 放射科病患用支架 (未滅菌)
Registration details
- Analysis ID
- 293b81036d39aff8a5893d5e939fba05
- License Form
- Ministry of Health Medical Device Import No. 014830
- Customs Code
- DHA09401483001
Company information
- Manufacturer
- MEDSPIRA LLC
- Manufacturer Country
- United States
- Authorized Representative
- Meide Medical Devices Co., Ltd
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Stent for Radiology Patients (P.1830)".
- 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
- Jan 08, 2015
- Expiry Date
- Jan 08, 2025
About this record
Access comprehensive regulatory information for "Medspira" 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 293b81036d39aff8a5893d5e939fba05 and manufactured by MEDSPIRA LLC. The authorized representative in Taiwan is Meide Medical Devices Co., Ltd.
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