Pure Global

TIGERLOOP™ BRAIDED POLYBLEND BLUE SUTURE, WHITE/GREEN, LOOPED, WITH STRAIGHT NEEDLE - FDA Registration MDR-07920

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.

Free Database
Powered by Pure Global AI
FDA Official Data
USA
MDR-07920
TIGERLOOP™ BRAIDED POLYBLEND BLUE SUTURE, WHITE/GREEN, LOOPED, WITH STRAIGHT NEEDLE
Registered medical device in Philippines
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Information
Product Name
TIGERLOOP™ BRAIDED POLYBLEND BLUE SUTURE, WHITE/GREEN, LOOPED, WITH STRAIGHT NEEDLE
Registration Number
MDR-07920
Manufacturer Details
Importer & Distribution
Importer/Distributor
Pacificsurgical, Inc.
Registration Dates
Issuance Date
May 08, 2025
Expiry Date
April 08, 2031