AccessGUDID - DEVICE: MEDCOMP TESIO CATHETERSMEDCOMP TESIO CATHETERS (00884908141214)

GUDID

Device Identifier (DI) Information

Brand Name: MEDCOMP TESIO CATHETERSMEDCOMP TESIO CATHETERS
Version or Model: DBFR-6S
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: DBFR-6S
Company Name: Medical Components, Inc.

Primary DI Number: 00884908141214
Issuing Agency: GS1
Commercial Distribution End Date: July 13, 2022
Device Count: 1
Labeler D-U-N-S® Number*: 038000253 *Terms of Use

Device Description: 10F BIO-FLEX®TESIO® CATHETERS W/STYLETCATHETERS W/ST (ARTERIAL CUFF-22CM FROM(ARTERIA TIP) (VENOUS CUFF-25CM FROMTIP) TIP)TIP)

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
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:	Yes
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
MSD	Catheter, hemodialysis, implanted

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
No Device Sizes

Device Record Status

Public Device Record Key: 8ab20c6a-d501-49f3-8cd5-9f118c4a4fb6
Public Version Date: July 21, 2022
Public Version Number: 3
DI Record Publish Date: August 14, 2019