AccessGUDID - DEVICE: Rescuer Disposable Resuscitation Cushion Mask (#4 Adult) (B00215060)

GUDID

Device Identifier (DI) Information

Brand Name: Rescuer Disposable Resuscitation Cushion Mask (#4 Adult)
Version or Model: 1506
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 1506
Company Name: B.L.S. Systems Limited

Primary DI Number: B00215060
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 200103823 *Terms of Use

Device Description: Rescuer Disposable Resuscitation Cushion Mask (#4 Adult

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?
57824	Resuscitator face mask, single-use	A non-sterile, flexible, form-shaped device that is placed over a patient's nose and mouth to direct ambient air, or medical oxygen (O2) and air, from a resuscitator to the upper airway and lungs. It is typically made of non-conductive sterilizable materials (e.g., silicone) that will create a gastight seal against the face. It will typically include a 15 mm and/or 22 mm connector and is available in a range of sizes (baby to adult). It will be directly attached to the resuscitator and held in place on the patient's face by the operator. This device is intended for use with a breathing resuscitator but may be used for the delivery of anaesthesia gases. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
BSJ	Mask, Gas, Anesthetic

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
Device Size Text, specify: #4 Adult

Device Record Status

Public Device Record Key: 4382abe5-e80d-4d6a-850d-89f678d7272a
Public Version Date: November 05, 2018
Public Version Number: 1
DI Record Publish Date: October 03, 2018