Vapotherm

Basic Information

• Brand Name: Vapotherm
• Primary DI: 00841737103448
• Version / Model: PF-OAM-MAS
• Company Name: VAPOTHERM, INC.
• Labeler DUNS: 040429050
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2020-06-15
• Public Version: 3
• Public Version Date: 2022-10-10
• Public Version Status: Update
• Public Device Record Key: e8ec8fee-50ba-4bee-bc7f-92244d173107

Device Description

Precision Flow Oxygen Assist Module, Massimo

Device Characteristics

• Single Use: No
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: MR Unsafe
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
QAV	High Flow/High Velocity Humidified Oxygen Delivery Device	Anesthesiology	868.5454	2
BTT	Humidifier, Respiratory Gas, (Direct Patient Interface)	Anesthesiology	868.5450	2

GMDN Terms

Code	Name	Definition	Implantable	Status
63057	Respiratory oxygen therapy physiologic monitor/gas regulator	An electrically-powered unit designed to be connected to a pulse oximeter sensor and used during the administration of oxygen (O2) to a spontaneously breathing patient, for: 1) continuous monitoring of physiologic parameters, especially haemoglobin oxygen saturation (SpO2); and 2) dynamic regulation of the amount of O2 delivered to the patient based on physiological parameter measurements. It is a computerized unit designed to interface between the O2 source and the patient and includes monitoring functionality, a graphic display, alarm(s), electronic gas valve, and integrated software.	No	Active
64303	Respiratory oxygen therapy pulse oximeter-regulator interface	An electrically-powered device designed to interface between a pulse oximeter probe and an electronic medical gas regulating unit during oxygen (O2) therapy, to continuously monitor haemoglobin oxygen saturation (SpO2), calculate the appropriate volume of O2 needed to be delivered to the patient based on SpO2 values, and transmit an electronic signal to the electronic O2 regulating unit. It includes a display, alarm(s), and integrated software; it does not come into direct contact with medical gases (i.e., does not include a gas regulator or tubing).	No	Active
57828	Professional high-flow respiratory unit, humidifying	An electrically-powered device designed to deliver high-flow (exceeding peak inspiratory flow) heated and humidified ambient air or air/oxygen to a patient in a peri-anaesthesia environment or experiencing a respiratory disorder [e.g., chronic obstructive pulmonary disease (COPD), bronchiectasis, xerostomia, and mucositis]. The gases are delivered as part of noninvasive ventilation (NIV) to the patient's airway via the nose/mouth or a tracheostoma. It consists of a gas flow generator, a heating element, and humidification chamber. It is intended to be used by a healthcare provider on a spontaneously breathing patient.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00841737103448	GS1