AccessGUDID - DEVICE: Fisher & Paykel Healthcare (09420012433060)

GUDID

Device Identifier (DI) Information

Brand Name: Fisher & Paykel Healthcare
Version or Model: SH870JHU
Commercial Distribution Status: In Commercial Distribution
Catalog Number: SH870JHU
Company Name: FISHER & PAYKEL HEALTHCARE LIMITED

Primary DI Number: 09420012433060
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 590153276 *Terms of Use

Device Description: HUMIDIFIER SH870 115V US

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?
48169	Insufflation gas conditioning system control unit	A mains electricity (AC-powered) device designed to be used together with a laparoscopic gas distention system or other gas source to condition the insufflation gas stream [typically carbon dioxide (CO2)] by automatically heating and humidifying the gas before introduction into the peritoneal cavity or a wound during laparoscopic or open surgery. It is electronically controlled and has controls and displays for the user to operate and monitor the gas conditioning process which happens within an interchangeable humidification chamber that is fitted to this device. The gas is delivered to the operative site via a dedicated heated tubing set.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
HIF	Insufflator, Laparoscopic

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
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: 6df25a3c-e6ce-49a3-892d-5408bfb9c3ac
Public Version Date: July 14, 2023
Public Version Number: 1
DI Record Publish Date: July 06, 2023