Home GUDID 10840199500182 Bayonet Suction Retractor
Primary DI 10840199500182
Brand Bayonet Suction Retractor
Company KOROS U.S.A., INC.
Model 7220-10
Device description Bayonet Suction Retractor 7mm tip 12 cm working length
Published 2022-01-31
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Product Codes# Code, Name table Code Name KWP Appliance, Fixation, Spinal Interlaminal
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWP Appliance, Fixation, Spinal Interlaminal Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00840199500185 Direct Marking GS1 0 10840199500182 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00840199500185 00840199500185 840199500185 0840199500185 10840199500182 10840199500182
GMDN Terms# Term, Definition table Term Definition External spinal fixation system An assembly of devices designed to stabilize adjacent segments (i.e., vertebrae) of the spine. It typically consists of an external plastic and/or metallic fixator and other external and/or implantable components, such as plates, rods, pins, and bone screws; it may also include some instruments appropriate for attaching the implants (e.g., screw drivers, wrenches, drills). The system is intended for temporary immobilization of segments of the spine in patients with fractures of the thoracic and/or lumbar spine and also for some patients suffering of segmental instability or chronic back pain. This is a reusable device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 Store in dry place at room temperature
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 007928633 Device count 1 Lot or batch true Serial number true 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 00193982239862 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982239886 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982239909 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982239923 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982239947 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982239961 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982240240 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982240363 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982240622 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982450151 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982450168 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982450175 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982450182 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982450199 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521134 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521141 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521158 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521165 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521172 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521189 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521196 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521202 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521219 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521226 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521233 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521240 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521257 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521264 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982521271 QUARTEX GLOBUS MEDICAL, INC. KWP 2026-08-14 00193982669638 CREO GLOBUS MEDICAL, INC. KWP 2026-08-14