Taiwan FDA registration b684b19e8f7ba2d09dcd651fd298924d
"Pearl Technology" Radiologic Patient Cradle (Non-Sterile)
TW: "沛爾" 放射科病患用支架 (未滅菌)
Taiwan·Risk Class 1·MD·PEARL TECHNOLOGY AG·Registered Jun 13, 2019 – Jun 13, 2024ExpiredRegistration details
- Analysis ID
- b684b19e8f7ba2d09dcd651fd298924d
- License Form
- Ministry of Health Medical Device Import No. 020545
- Customs Code
- DHA09402054501
Company information
- Manufacturer
- PEARL TECHNOLOGY AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- HSIEN TAI INSTRUMENTS 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
- Jun 13, 2019
- Expiry Date
- Jun 13, 2024
About this record
Access comprehensive regulatory information for "Pearl Technology" 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 b684b19e8f7ba2d09dcd651fd298924d and manufactured by PEARL TECHNOLOGY AG. The authorized representative in Taiwan is HSIEN TAI INSTRUMENTS CO., LTD..
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