AccessGUDID - DEVICE: Intellijet (00885556602553)

GUDID

Device Identifier (DI) Information

Brand Name: Intellijet
Version or Model: 7205076
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 7205076
Company Name: Smith & Nephew, Inc.

Primary DI Number: 00885556602553
Issuing Agency: GS1
Commercial Distribution End Date: April 05, 2017
Device Count: 1
Labeler D-U-N-S® Number*: 045483575 *Terms of Use

Device Description: PEDESTAL POLE INTELIJET

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?
35616	Endoscopic video imaging system	An assembly of mains electricity (AC-powered) devices designed to obtain, transmit, and display video images during an endoscopic procedure. It typically consists of one or more video endoscopes, an endoscopic camera, camera control unit, light source with light cables, video recorder, imaging units with perhaps a colour compensation device, a distention unit, and a visual display unit (VDU), all of which is typically placed/mounted onto a trolley (cart) that can be moved to different examination/treatment rooms.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
FWF	CAMERA, TELEVISION, ENDOSCOPIC, WITHOUT AUDIO

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: 76d3025c-3232-4bf5-8f8f-a107656f8a2c
Public Version Date: September 07, 2023
Public Version Number: 3
DI Record Publish Date: October 22, 2015