AccessGUDID - DEVICE: Fisher & Paykel Healthcare (09420012477910)

GUDID

Device Identifier (DI) Information

Brand Name: Fisher & Paykel Healthcare
Version or Model: AA451J
Commercial Distribution Status: In Commercial Distribution
Catalog Number: AA451J
Company Name: FISHER & PAYKEL HEALTHCARE LIMITED

Primary DI Number: 09420012477910
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 590153276 *Terms of Use

Device Description: Optiflow Oxygen Kit

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":	Yes
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?
65351	Humidified oxygen administration set	A collection of consumable devices designed to work together to deliver humidified pure oxygen (O2) or an O2 enriched gas to a mask or nasal cannula during oxygen administration to a patient (e.g., oxygen therapy, anaesthesia). It includes oxygen administration tubing (inspiratory line, dryline) which includes an electronic component (e.g., temperature sensor, heating wire), an inspiratory line humidification chamber, and may include a water bag. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
BTT	Humidifier, Respiratory Gas, (Direct Patient Interface)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K233821	000

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 -10 and 50 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 415fd998-d5c5-461f-9747-a2472751c53e
Public Version Date: September 19, 2024
Public Version Number: 1
DI Record Publish Date: September 11, 2024