Home GUDID 15060557440331 Galaxy II Surgical Retractor
Primary DI 15060557440331
Brand Galaxy II Surgical Retractor
Company MOSAIC SURGICAL LIMITED
Model JUNE3000sb5
Device description Galaxy II Snowman Kit (5mm Semi-Blunt Stays)
Published 2026-03-26
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 15060557440331 Primary GS1 0 05060557440334 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 15060557440331 15060557440331 05060557440334 05060557440334 5060557440334
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 00199150083107 Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC. GAD 2026-07-30 00199150083879 Medtronic Reusable Instruments MEDTRONIC SOFAMOR DANEK, INC. GAD 2026-07-30 00810143904659 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143904680 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143904697 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143904703 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143904710 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143904727 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143904918 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143904925 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143904932 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143904949 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143904956 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143905045 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143905380 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143906387 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143906394 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143906400 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143907001 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143907094 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143908374 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143908558 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143908794 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143908800 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143908817 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143908824 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143908831 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143908848 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810143909609 SURGIPROS Surgipros, LLC GAD 2026-07-30 00810212930343 SURGIPROS Surgipros, LLC GAD 2026-07-30