AccessGUDID - DEVICE: Mediox (00850054612366)

GUDID

Device Identifier (DI) Information

Brand Name: Mediox
Version or Model: Lengthening children type (M)
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Mediox Medical Service Ltd

Primary DI Number: 00850054612366
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 118843955 *Terms of Use

Device Description: Nebulizer

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":	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?
35142	Aerosol face mask, rebreathing, single-use	A flexible, form-shaped device that is placed over the nose and mouth to deliver aerosolized particles/gases to a patient's airway. It is typically used in conjunction with a nebulizer or medicine chamber spacer for the delivery of medication in either a healthcare or home setting. It is made of high-grade resins or other materials to produce a soft, flexible mask that will create an airtight seal against the patient's face. It may include a headstrap and is available in a range of sizes. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
CCQ	Nebulizer, Medicinal, Non-Ventilatory (Atomizer)

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: ca2cfa1f-2ad2-4cb3-b3b7-e6bf179bf6d6
Public Version Date: September 01, 2023
Public Version Number: 1
DI Record Publish Date: August 24, 2023