Home GUDID M2484596R1 Omni-Tract®
Primary DI M2484596R1
Brand Omni-Tract®
Company INTEGRA LIFESCIENCES CORPORATION
Model 4596R
Catalog number 4596R
Device description Omni-Tract® Mulier Hip Retractor, 2in x 2.5in (5.1cm x 6.4cm)
Published 2018-02-23
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use false Product Codes# Code, Name table Code Name FGN RETRACTOR, NON-SELF-RETAINING
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class FGN Retractor, Non-Self-Retaining Gastroenterology, Urology 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10381780270751 Primary GS1 0 M2484596R1 Secondary HIBCC 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10381780270751 10381780270751
GMDN Terms# Term, Definition table Term Definition Surgical retraction system, reusable A frame-like assembly of surgical instruments/devices intended to be used to create a self-locking, self-retaining mechanism to temporarily part tissue (e.g., hold the edges of an incision open) to expose internal tissues or organs for access during open surgery; is not intended for neurosurgery or ophthalmic surgery. It includes a mounting frame (e.g., bar, ring) and a number of detachable retracting blades, may include additional features (e.g., ratchet mechanisms, fibreoptic lights), and might be intended to be mounted to the operating table or be non-fixed. It is typically made of high-grade stainless steel and synthetic materials. This is a reusable device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 963856096 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published B803NL97020450 ORTHOMED ORTHO-MED, INC. FGN 2026-06-25 B803COD5045680 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803COD5045690 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803COD5045700 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803COD5045710 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1107210 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1107230 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1107370 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1107390 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1108340 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1108360 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803MA1108370 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020100 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020110 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020120 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020130 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020140 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020150 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020200 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020210 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020220 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020230 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020240 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020250 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020260 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020300 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020310 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020320 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020330 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23 B803NL97020340 ORTHOMED ORTHO-MED, INC. FGN 2026-06-23
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