Home GUDID 15060557440447 Galaxy II Surgical Retractor
Primary DI 15060557440447
Brand Galaxy II Surgical Retractor
Company MOSAIC SURGICAL LIMITED
Model GX30
Device description Galaxy II HandMe Kit
Published 2026-04-09
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Sterile true
Single use true Product Codes# Code, Name table Code Name FFO Retractor, Self-Retaining GAD Retractor HDL Retractor, Vaginal KAL Retractor, Ent
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class FFO Retractor, Self-Retaining Gastroenterology, Urology 1 GAD Retractor General, Plastic Surgery 1 HDL Retractor, Vaginal Obstetrics/Gynecology 1 KAL Retractor, Ent Ear, Nose, Throat 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 15060557440447 Primary GS1 0 05060557440440 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 15060557440447 15060557440447 05060557440440 05060557440440 5060557440440
GMDN Terms# Term, Definition table Term Definition Surgical retraction system, single-use A sterile, 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 single-use device.
Regulatory Flags# DUNS number 222357455 Device count 10 Premarket exempt true Lot or batch true Manufacturing date on label true Expiration date on label true No natural rubber latex true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00190776404239 Millennium Avalign Technologies, Inc. GAD 2026-07-24 00190776422042 Millennium Avalign Technologies, Inc. GAD 2026-07-24 00190776422103 Millennium Avalign Technologies, Inc. GAD 2026-07-24 00190776422134 Millennium Avalign Technologies, Inc. GAD 2026-07-24 B382SD907394200 Surgical Direct Surgical Direct, Inc. GAD 2026-07-24 B382SD907581320 Surgical Direct Surgical Direct, Inc. FFO 2026-07-24 B382SD914172160 Surgical Direct Surgical Direct, Inc. GAD 2026-07-24 B382SD9141731000 Surgical Direct Surgical Direct, Inc. GAD 2026-07-24 B382SD9141781300 Surgical Direct Surgical Direct, Inc. GAD 2026-07-24 00190776421977 Millennium Avalign Technologies, Inc. GAD 2026-07-23 00190776403942 Millennium Avalign Technologies, Inc. KAL 2026-07-22 00198506091926 ELMED INCORPORATED ELMED INCORPORATED GAD 2026-07-22 00198506092015 ELMED INCORPORATED ELMED INCORPORATED GAD 2026-07-22 00198506093685 ELMED INCORPORATED ELMED INCORPORATED GAD 2026-07-22 00841731153104 ARTEMIS FUZE VILEX LLC GAD 2026-07-22 00841731153111 ARTEMIS FUZE VILEX LLC GAD 2026-07-22 B8038600980 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B8038600990 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B803860120L0 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B8038601250 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B8039018420 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B8039018430 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B8039018840 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B8039030020 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B803903220010 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B803903220020 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B8039401000 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B8039601360 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B8039601370 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22 B8039601390 ORTHOMED ORTHO-MED, INC. GAD 2026-07-22