AccessGUDID - DEVICE: BougieCap (04260206310822)

GUDID

Device Identifier (DI) Information

Brand Name: BougieCap
Version or Model: 8
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 400.31.02
Company Name: Ovesco Endoscopy AG

Primary DI Number: 04260206310822
Issuing Agency: GS1
Commercial Distribution End Date: September 30, 2022
Device Count: 1
Labeler D-U-N-S® Number*: 344007369 *Terms of Use

Device Description: The BougieCap is for dilation of strictures in the upper gastrointestinal tract • the transparent cap allows direct visual control during the dilation • the tension on the tissue is visible while passing the stricture, thereby avoiding overstretching • reduced procedure time due to less intrument change • evaluation can be done directly after the dilation thanks to the attached transparent cap • two lateral holes for air insufflation and suction • one centered hole for the insertion of a guide wire

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":	Yes
For Single-Use:	Yes
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?
62109	Endoscopic gastrointestinal stenosis dilator	A sterile invasive device intended to be used to dilate or expand a narrowing lesion (e.g., oesophageal stricture, stenosis) in the lumen of the gastrointestinal [GI] tract, under endoscopic visualization. It is made of transparent synthetic polymer material and is available in various forms (e.g., a slender hollow tube through which is passed the endoscope before introduction into the GI tract, or a tapered cap applied to the distal end of the endoscope); the dilator is advanced through the lesion site with direct visualization through the endoscope. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KNQ	Dilator, Esophageal

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: Yes
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
Device Size Text, specify: mounting depht of the cap: 5 mm
Device Size Text, specify: for endoscopes with diameter 5.5 - 6 mm
Length: 16.6 Millimeter
Outer Diameter: 8.1 Millimeter

Device Record Status

Public Device Record Key: 4c46d5b4-e0f1-415f-afd3-0cb0cdb43088
Public Version Date: September 30, 2022
Public Version Number: 3
DI Record Publish Date: October 05, 2018