Home GUDID 05030267095841
N/A
Primary DI 05030267095841
Brand N/A
Company INTERSURGICAL INCORPORATED
Model 2320030
Device description MANUAL FILL HUMIDIFICATION CHAMBER
Published 2016-09-24
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 BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class BTT Humidifier, Respiratory Gas, (Direct Patient Interface) Anesthesiology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 05030267095841 Package GS1 30 In Commercial Distribution 05030267095834 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 05030267095841 05030267095841 5030267095841 05030267095834 05030267095834 5030267095834
GMDN Terms# Term, Definition table Term Definition Heated respiratory humidifier A mains electricity (AC-powered) device designed to heat and humidify air/oxygen inspired by a patient to help maintain the mucous membranes of the respiratory tract typically during periods of prolonged respiratory support/therapy (e.g., mechanical ventilation, BPAP/CPAP therapy). The heated/humidified gases are delivered to the patient's airway and lungs via the nose/mouth or a tracheostoma in association with a parent respiratory device (e.g., ventilator, BPAP/CPAP unit). The humidifier typically includes a heating element and provisions for attaching a humidification chamber and tubing set.
Regulatory Flags# DUNS number 785952607 Device count 1 DM exempt true Premarket exempt false HCT/P false Kit true 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 false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 05030267169870 I-GEL®, SUPRAGLOTTIC AIRWAY, SIZE 1.0, NEONATE, 2-5KG (US) 8201030 2026-06-02 05030267169894 I-GEL®, SUPRAGLOTTIC AIRWAY, SIZE 2.0, SMALL PAEDIATRIC, 10-25KG (US) 8202030 2026-06-02 05030267169917 I-GEL®, SUPRAGLOTTIC AIRWAY, SIZE 3, SMALL ADULT, 30-60KG (US) 8203030 2026-06-02 05030267169931 I-GEL®, SUPRAGLOTTIC AIRWAY, SIZE 4, MEDIUM ADULT, 50-90KG (US) 8204030 2026-06-02 05030267169955 I-GEL®, SUPRAGLOTTIC AIRWAY, SIZE 5, LARGE ADULT, 90+KG (US) 8205030 2026-06-02 05030267169979 I-GEL®, SUPRAGLOTTIC AIRWAY, SIZE 1.5, INFANT, 5-12KG (US) 8215030 2026-06-02 05030267169993 I-GEL®, SUPRAGLOTTIC AIRWAY, SIZE 2.5, LARGE PAEDIATRIC, 25-35KG (US) 8225030 2026-06-02 05030267170012 I-GEL® PLUS-A, SUPRAGLOTTIC AIRWAY, SIZE 3, SMALL ADULT, 30-60KG (US) 8903030 2026-06-02 05030267170036 I-GEL® PLUS-A, SUPRAGLOTTIC AIRWAY, SIZE 4, MEDIUM ADULT, 50-90KG (US) 8904030 2026-06-02 05030267170050 I-GEL® PLUS-A, SUPRAGLOTTIC AIRWAY, SIZE 5, LARGE ADULT, 90+KG (US) 8905030 2026-06-02 05030267089123 FIXED ELBOW, 15M - 22M/15F - STERILE 1997000S 2026-04-28 05030267169542 SENTRI™ INTERSURGICAL ECOLITE™, ADULT, MASK WITH CO2 MONITORING LINE, FILTER 1143035 2026-04-21 05030267169573 SENTRI™ INTERSURGICAL ECOLITE™, ADULT, MASK WITH TUBE, 2.1M USA ONLY 1141035 2026-04-21 05030267169597 SENTRI™ INTERSURGICAL ECOLITE™, ADULT, MASK WITH CO2 MONITORING LINE, FILTER 1143038 2026-04-21 05030267169634 SENTRI™ INTERSURGICAL ECOLITE™, ADULT, MASK WITH CO MONITORING LINE AND TUBE 1142035 2026-04-21 05030267056057 Y-PIECE 22M, 22M, 22M/15F 1900000 2021-10-12 05030267056095 Y-PIECE 22M, 22M, 22M/15F WITH PORTS 1901000 2021-10-12 05030267056118 Y-PIECE 15M, 15M, 15F 1902000 2021-10-12 05030267056132 Y-PIECE 15M, 15M, 22M/15F + 7.6MM PORTS, PAEDIATRIC 1903000 2021-10-12 05030267056347 PARALLEL Y-PIECE, 22MM 1926000 2021-10-12
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