AccessGUDID - DEVICE: ZephyrLIFE Hospital (10884521712904)

GUDID

Device Identifier (DI) Information

Brand Name: ZephyrLIFE Hospital
Version or Model: Software Hospital
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: Software Hospital
Company Name: ZEPHYR TECHNOLOGY LLC

Primary DI Number: 10884521712904
Issuing Agency: GS1
Commercial Distribution End Date: September 24, 2016
Device Count: 1
Labeler D-U-N-S® Number*: 796678527 *Terms of Use

Device Description: ZephyrLIFE Hospital Application Software Application?

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?
58494	Electrosurgical return electrode, single-use	A dispersive conductor intended to be fastened to a patient and connected to an electrosurgical/radio-frequency ablation system generator, to allow return of electrical current from the patient to the generator during an electrosurgical procedure. It has a large surface area and is fastened to the patient's body typically where the greatest surface area can be covered in closest proximity to the surgical site. It will typically be designed with permanently attached leads. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DRG	TRANSMITTERS AND RECEIVERS, PHYSIOLOGICAL SIGNAL, RADIOFREQUENCY

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: bdeab43d-d1ce-4cf9-bd16-b14c64075a06
Public Version Date: January 29, 2024
Public Version Number: 3
DI Record Publish Date: September 24, 2016