Stryker Air™+ All-Inside Meniscal Repair System - HSA Registration DE0509721
Access comprehensive regulatory information for Stryker Air™+ All-Inside Meniscal Repair System in the Singapore medical device market through Pure Global AI's free database. This CLASS C medical device is registered under HSA registration number DE0509721 and owned by Stryker Endoscopy. The device was registered on September 03, 2024.
This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.
The AIR™+ All-Inside Meniscal Repair Device is intended for use as a suture retention device to facilitate percutaneous or endoscopic soft tissue procedures. The AIR™+ All-Inside Meniscal Repair Device is indicated for use in meniscal repairs and allograft transplant procedures. The AIR™+ All-Inside Meniscal Repair Device is intended to be used for anchoring the allograft to the meniscal rim during allograft transplant procedures.