Philippines FDA registration MDR-08153
HI-TORQUE PILOT 150 GUIDE WIRE
Device information
- Product Name
- HI-TORQUE PILOT 150 GUIDE WIRE
- Registration Number
- MDR-08153
Manufacturer details
- Manufacturer
- Abbott Vascular
- Country of Origin
- USA
Importer & distribution
- Importer/Distributor
- Abbott Laboratories
Registration dates
- Issuance Date
- April 01, 2020
- Expiry Date
- May 27, 2025
About this record
Access comprehensive regulatory information for HI-TORQUE PILOT 150 GUIDE WIRE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08153 and manufactured by Abbott Vascular in USA. The device was registered on April 01, 2020.
This page provides complete registration details including manufacturer information, importer/distributor details (Abbott Laboratories), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.
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