AccessGUDID - DEVICE: Dualator Vessel Dilator 10-12 F x 15 cm (00801741012471)

GUDID

Device Identifier (DI) Information

Brand Name: Dualator Vessel Dilator 10-12 F x 15 cm
Version or Model: 5582000
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 5582000
Company Name: Bard Access Systems, Inc.

Primary DI Number: 00801741012471
Issuing Agency: GS1
Commercial Distribution End Date: June 27, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 044611812 *Terms of Use

Device Description: DUALATOR VESSEL DILATOR 10-12 FR. 15cm

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:	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?
37278	Double-lumen haemodialysis catheter, implantable	An implantable, flexible, double-lumen tube intended to be used for chronic or long-term (> 30 days) vascular access, primarily during haemodialysis, to conduct blood from a patient and returning it after extracorporeal circulation; it may also be used during haemoperfusion and/or apheresis. It is intended for coaxial flow of blood, may be radiopaque, coated with heparin to prevent thrombus formation, and/or include a silver-coated sleeve to retard bacterial growth; devices dedicated to catheter introduction/function (e.g., introducer needle) may be included.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
LFJ	CATHETER, SUBCLAVIAN

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Length: 15 Centimeter
Catheter Gauge: 12 French
Catheter Gauge: 10 French
Catheter Gauge: 11 French

Device Record Status

Public Device Record Key: 0a0b4cef-fdd1-470b-90b1-f110c8095a69
Public Version Date: December 19, 2024
Public Version Number: 4
DI Record Publish Date: May 29, 2017