AccessGUDID - DEVICE: DELTA-FLOW (H6711002040)

GUDID

Device Identifier (DI) Information

Brand Name: DELTA-FLOW
Version or Model: Male Flow-Through Configuration
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 100-204
Company Name: UTAH MEDICAL PRODUCTS, INC.

Primary DI Number: H6711002040
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 094651270 *Terms of Use

Device Description: CONTINUOUS FLUSH DEVICE, 3CC/HR FLOW RATE, MALE, BLUE, W/TAB

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?
35511	Vascular catheter flush valve, continuous	A specialized, sterile, Y-piece device intended to be connected in an infusion line to an indwelling catheter and provide for the connection of a second infusion source. The second source usually serves to maintain a low keep vein open (KVO) flow in the catheter to prevent clotting. This device (the flush valve) may be equipped with a manually-operated mechanism to permit flushing of the line at a free-flow rate. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KRA	Catheter, Continuous Flush

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K780479	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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: Flow Rate - 3 cc/hr

Device Record Status

Public Device Record Key: 2108017c-6ab2-4405-920a-ac314f3e86ac
Public Version Date: December 18, 2019
Public Version Number: 4
DI Record Publish Date: September 23, 2016