AccessGUDID - DEVICE: Breathing bag set with PEEP valve, disposable (04049098000468)

GUDID

Device Identifier (DI) Information

Brand Name: Breathing bag set with PEEP valve, disposable
Version or Model: MU04776
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: DRAEGER MEDICAL SYSTEMS, INC.

Primary DI Number: 04049098000468
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 788289952 *Terms of Use

Device Description: No description.

Device Characteristics

What MRI safety information does the labeling contain?	MR Unsafe
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":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
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?
35121	Transport infant incubator	An electrically-powered unit designed to provide an enclosed controlled environment to maintain appropriate temperature, and in some cases humidity levels, mainly for premature infants and other newborns who cannot effectively regulate their body temperature; it is typically on wheels and is designed for transporting infants either outside or within the healthcare facility. It typically consists of a clear removable/openable plastic hood with a mattress and operates using mains electricity (AC-powered) when not in use for transportation; some types may be supplied with an equipment rack. During transport, it is connected to an ambulance electrical outlet or is battery-powered.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
BTM	Ventilator, Emergency, Manual (Resuscitator)

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: 55b6a2fe-54f6-4e50-8b09-9f9d23a8cfb1
Public Version Date: September 19, 2024
Public Version Number: 3
DI Record Publish Date: October 24, 2015