AccessGUDID - DEVICE: Falcon (00724995182663)

GUDID

Device Identifier (DI) Information

Brand Name: Falcon
Version or Model: 00711141
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 00711141
Company Name: US Endoscopy

Primary DI Number: 00724995182663
Issuing Agency: GS1
Commercial Distribution End Date: November 28, 2022
Device Count: 1
Labeler D-U-N-S® Number*: 627879687 *Terms of Use
Previous DI: 00816765011171

Device Description: The Falcon rotatable retrieval basket is used to retrieve foreign bodies, tissue specimens, stones or calculi in endoscopic procedures of the gastrointestinal tract.

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?
46454	Gastrointestinal/airway foreign body retrieval basket, single-use	A flexible device intended to access the gastrointestinal (GI) tract, and/or the airway tree, via the working channel of an appropriate endoscope to atraumatically remove foreign bodies during an endoscopic procedure; it may in addition be intended for removal of severed polyps and tissue samples (biopsy). It is typically designed with a long, thin, flexible body that has an expandable basket at the distal end in which objects are caught for extraction. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FGO	DISLODGER, STONE, FLEXIBLE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K962676	000

Device Exempt from Premarket Submission: No 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
Special Storage Condition, Specify: Keep Dry

Clinically Relevant Size

[?]

Size Type Text
Length: 230 Centimeter
Width: 35 Millimeter
Outer Diameter: 2.5 Millimeter

Device Record Status

Public Device Record Key: c42f23ba-f613-419b-8b47-6fca4571c97e
Public Version Date: November 29, 2022
Public Version Number: 4
DI Record Publish Date: March 19, 2020