Philippines FDA registration MDR-07920

TIGERLOOP™ BRAIDED POLYBLEND BLUE SUTURE, WHITE/GREEN, LOOPED, WITH STRAIGHT NEEDLE

Philippines·Arthrex, Inc, - 1370 Creekside Boulevar, Naples, Florida 34108-1945, USA·USA·Issued May 08, 2025 – April 08, 2031

Device information

Product Name: TIGERLOOP™ BRAIDED POLYBLEND BLUE SUTURE, WHITE/GREEN, LOOPED, WITH STRAIGHT NEEDLE
Registration Number: MDR-07920

Manufacturer details

Manufacturer: Arthrex, Inc, - 1370 Creekside Boulevar, Naples, Florida 34108-1945, USA
Country of Origin: USA

Importer & distribution

Importer/Distributor: Pacificsurgical, Inc.

Registration dates

Issuance Date: May 08, 2025
Expiry Date: April 08, 2031

About this record

Access comprehensive regulatory information for TIGERLOOP™ BRAIDED POLYBLEND BLUE SUTURE, WHITE/GREEN, LOOPED, WITH STRAIGHT NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07920 and manufactured by Arthrex, Inc, - 1370 Creekside Boulevar, Naples, Florida 34108-1945, USA in USA. The device was registered on May 08, 2025.

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.