AccessGUDID - DEVICE: N2O HOSE DISS F X HNDTWST 5 FT (00816711022909)

GUDID

Device Identifier (DI) Information

Brand Name: N2O HOSE DISS F X HNDTWST 5 FT
Version or Model: 92305289-5
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 92305289-5
Company Name: PARKER-HANNIFIN CORPORATION

Primary DI Number: 00816711022909
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 004175550 *Terms of Use

Device Description: N2O HOSE DISS F X HNDTWST 5 FT

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:	No
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?
37931	Nitrous oxide quick-connect coupling, female	A female connecting device used to accept a male nitrous oxide (N2O) connector to connect two devices together to provide a continuous passageway for the delivery of N2O. It has safety features such as a specific mechanical mating pattern, colour coding and a dedicated tube diameter connection to prevent wrong connection and allow a user to rapidly connect and disconnect N2O dependent devices. It can be attached, e.g., to an N2O regulator or an N2O extension tubing. It can be designed as a diameter-indexed safety system (DISS) connector or a non-interchangeable screw-threaded (NIST) connector. This is not a nitrous oxide terminal unit.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
BYX	Tubing, Pressure And Accessories

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: a3a208e7-140c-4dcc-bf50-9c9c503392e7
Public Version Date: November 23, 2022
Public Version Number: 1
DI Record Publish Date: November 15, 2022