AccessGUDID - DEVICE: AirLife (10885403039232)

GUDID

Device Identifier (DI) Information

Brand Name: AirLife
Version or Model: 002500
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 002500
Company Name: Carefusion Corporation

Primary DI Number: 10885403039232
Issuing Agency: GS1
Commercial Distribution End Date: March 31, 2022
Device Count: 1
Labeler D-U-N-S® Number*: 830432451 *Terms of Use

Device Description: Airlife™ Misty Finity™ Large Volume Continuous Nebulizer With 7' (2.1 m) Crush Resistant Oxygen Tubing

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?
12716	Therapeutic agent vaporizer, benchtop	An assembly of devices intended to be used in the home and clinical settings to vaporize (through heating) medication/fluids (e.g., pharmacological drugs, medical cannabis) for inhalation by a patient, typically to treat/manage a respiratory disorder [e.g., chronic obstructive pulmonary disease (COPD), cystic fibrosis (CF)] or various other conditions (e.g., chronic pain). It includes an electrically-powered generator, a reservoir, a heating element, dosing capsules, and a hand-held inhalation compartment (e.g., inflatable balloon with mouthpiece).¿¿It is designed to be placed on a benchtop/flat surface during use.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
CAF	NEBULIZER (DIRECT PATIENT INTERFACE)

FDA Premarket Submission

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

Device Exempt from Premarket Submission: No 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: e0f2f71d-19bc-492c-985a-512de0ee210a
Public Version Date: September 24, 2025
Public Version Number: 5
DI Record Publish Date: September 01, 2016