Home GUDID 10380657409706 ALCON
Primary DI 10380657409706
Brand ALCON
Company Alcon Laboratories, Inc.
Model 8065740970
Device description SILICONE I/A TIP STRAIGHT
Published 2017-06-08
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 NKK NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class NKK Needle, Hypodermic, Single Lumen, Reprocessed General Hospital 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10380657409706 Package GS1 4 In Commercial Distribution 00380657409709 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 10380657409706 10380657409706 00380657409709 00380657409709 380657409709 0380657409709
GMDN Terms# Term, Definition table Term Definition Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable A rigid or semi-rigid tube (non-illuminating) designed to be inserted into the eye to facilitate infusion, irrigation, and/or aspiration of fluids/gases during ophthalmic surgery (e.g., phacoemulsification, vitreoretinal surgery, sub-Tenon’s anaesthesia, capsule polishing). It is a single- or multi-lumen device, typically made of high-grade stainless steel, and may include a length of flexible tubing. It may be blunt, or include a sharp angled tip/hook (e.g., irrigating cystotome for capsulotomy), however it does not have a sharp bevelled end for initial puncture of the eye (i.e., not a needle). This is a reusable device intended to be sterilized prior to use.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 008018525 Device count 1 DM exempt true Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false 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 G079C5020000450 Golden Isles Pedicle Screw System Intelivation, LLC NKK 2022-10-03 00850033297010 Kova Plastics Alltrista Plastics LLC NKK 2021-07-29 00380657510122 INTREPID® Alcon Laboratories, Inc. NKK 2020-09-02 00380657510139 INTREPID® Alcon Laboratories, Inc. NKK 2020-09-02 00380658175016 ULTRAFLOW Alcon Laboratories, Inc. NKK 2018-02-28 00380657409693 ALCON Alcon Laboratories, Inc. NKK 2017-06-08 00380657409709 ALCON Alcon Laboratories, Inc. NKK 2017-06-08 10380657409690 ALCON Alcon Laboratories, Inc. NKK 2017-06-08 00380657517954 ULTRA FLOW Alcon Laboratories, Inc. NKK 2017-06-07 00380658170011 ULTRA FLOW Alcon Laboratories, Inc. NKK 2017-06-07 00380658172015 ULTRA FLOW Alcon Laboratories, Inc. NKK 2017-06-07
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