Philippines FDA registration MDR-10178A
ARTHREX FASTHREAD PEEK INTERFERENCE SCREW, WITH DISPOSABLE SHEATH
Philippines·Arthrex, Inc.·USA·Issued August 06, 2020 – August 06, 2021Device information
- Product Name
- ARTHREX FASTHREAD PEEK INTERFERENCE SCREW, WITH DISPOSABLE SHEATH
- Registration Number
- MDR-10178A
Manufacturer details
- Manufacturer
- Arthrex, Inc.
- Country of Origin
- USA
Importer & distribution
- Importer/Distributor
- Pacific Surgical, Inc.
Registration dates
- Issuance Date
- August 06, 2020
- Expiry Date
- August 06, 2021
About this record
Access comprehensive regulatory information for ARTHREX FASTHREAD PEEK INTERFERENCE SCREW, WITH DISPOSABLE SHEATH in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10178A and manufactured by Arthrex, Inc. in USA. The device was registered on August 06, 2020.
This page provides complete registration details including manufacturer information, importer/distributor details (Pacific Surgical, 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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