Home GUDID 50788942595000 Portex
Primary DI 50788942595000
Brand Portex
Company ICU MEDICAL, INC.
Model 55-9500
Published 2016-10-11
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 true Product Codes# Code, Name table Code Name CBD BOTTLE, COLLECTION, BREATHING SYSTEM (CALIBRATED)
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class CBD Bottle, Collection, Breathing System (Calibrated) General Hospital 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 50788942595000 Package GS1 36 In Commercial Distribution 10788942595002 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 50788942595000 50788942595000 10788942595002 10788942595002
GMDN Terms# Term, Definition table Term Definition ENT examination/treatment system An assembly of devices intended to support a patient in a supine or reclining position and provide specialized features for an ear/nose/throat (ENT) examination or treatment. It typically includes a table and/or chair and functional components such as a suction/blowing apparatus, equipment drawers, and a mirror heater.
Regulatory Flags# DUNS number 118380146 Device count 1 DM exempt false Premarket exempt false 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 true Sterilization required before use false Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00841737104384 Vapotherm VAPOTHERM, INC. CBD 2021-05-03 10788942595002 Portex ICU MEDICAL, INC. CBD 2016-10-11