AccessGUDID - DEVICE: AirLife (10885403220791)

GUDID

Device Identifier (DI) Information

Brand Name: AirLife
Version or Model: 2K7203
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 2K7203
Company Name: Carefusion Corporation

Primary DI Number: 10885403220791
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: Neonatal Manual Resuscitator; 40" (1.0m) Oxygen Resevoir Tubing, Neonatal Mask, Pressure Limiting Valve with lock, Pressure Manometer, 7' O2 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:	Yes
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?
36086	Pulmonary resuscitator, manual, single-use	A non-sterile, hand-operated device designed to provide or assist ventilation in patients who are apnoeic or exhibit inadequate respiration. It typically employs entrained ambient air and includes a large flexible chamber that is hand-ventilated, a gas reservoir, tubing, and a connector for attachment to a mask or endotracheal (ET) tube; oxygen (O2) from an O2 source may also be connected when necessary. It is used used by emergency medical services (EMS) in ambulances, intensive care units (ICU), during internal patient transfer, accident and emergency (A&E), mass casualty incidents (MCI), and is generally placed strategically throughout a hospital. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OEV	Cardiopulmonary Resuscitation Aid Kit

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
Storage Environment Temperature: between -40 and 123 Degrees Fahrenheit

Clinically Relevant Size

[?]

Size Type Text
Weight: 240.00 Gram
Total Volume: 280.00 Milliliter

Device Record Status

Public Device Record Key: 14bd8024-ac71-4acc-9c57-cfe02dac2711
Public Version Date: May 21, 2024
Public Version Number: 3
DI Record Publish Date: October 24, 2015