AccessGUDID - DEVICE: AirLife™ (10190752116689)

GUDID

Device Identifier (DI) Information

Brand Name: AirLife™
Version or Model: 001363
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 001363
Company Name: VYAIRE MEDICAL, INC.

Primary DI Number: 10190752116689
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 080456871 *Terms of Use

Device Description: AirLife™ Adult Venturi Style Mask Vinyl, Under-the-Chin Style Adult Mask, 6 inch (15 cm) Flextube, Six Diluter Jets, Nebulizer Hood, 7 feet (2.1 m) Oxygen Tubing and U/Connect-It Adapter

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
35171	Rebreathing oxygen face mask	A non-sterile, flexible, form-shaped device designed to be placed over the nose and mouth to deliver a proportional mixture of air/oxygen (O2) to a patient's airway. It is made of non-conductive, soft, flexible polymers available in a range of sizes, and designed to create an airtight seal against the patient's face. The device may include tubing and various valves and connectors which may allow for connection to a central vacuum system to enable scavenging of residual (waste) anaesthetic gas from a patient in recovery; other respiratory equipment (e.g., nebulizer, humidifier, CPAP device) is not included. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
CAT	CANNULA, NASAL, OXYGEN

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 8b00aa67-7939-4991-9efa-3f370dfd7192
Public Version Date: February 12, 2020
Public Version Number: 1
DI Record Publish Date: February 04, 2020