Philippines FDA registration MDR-10049E
ARTHREX® SYNDESMOSIS TIGHTROPE® XP IMPLANT, STAINLESS STEEL
Philippines·Arthrex, Inc.·USA·Issued July 23, 2020 – July 23, 2020Device information
- Product Name
- ARTHREX® SYNDESMOSIS TIGHTROPE® XP IMPLANT, STAINLESS STEEL
- Registration Number
- MDR-10049E
Manufacturer details
- Manufacturer
- Arthrex, Inc.
- Country of Origin
- USA
Importer & distribution
- Importer/Distributor
- Pacificsurgical, Inc.
Registration dates
- Issuance Date
- July 23, 2020
- Expiry Date
- July 23, 2020
About this record
Access comprehensive regulatory information for ARTHREX® SYNDESMOSIS TIGHTROPE® XP IMPLANT, STAINLESS STEEL in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10049E and manufactured by Arthrex, Inc. in USA. The device was registered on July 23, 2020.
This page provides complete registration details including manufacturer information, importer/distributor details (Pacificsurgical, Inc.), 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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