AccessGUDID - DEVICE: INTERLINK/CONTINU-FLO (00085412017853)

GUDID

Device Identifier (DI) Information

Brand Name: INTERLINK/CONTINU-FLO
Version or Model: 3C0091
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 3C0091
Company Name: BAXTER INTERNATIONAL INC.

Primary DI Number: 00085412017853
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 005146311 *Terms of Use

Device Description: CONTINU-FLO Solution Set, 2 Injection Sites, Male Luer Lock Adapter, Stopcock Extension Set, Large Bore Stopcock with Rotating Male Luer Lock, Extension Set, Injection Site, Male Luer Lock Adapter with Retractable Collar

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?
32172	Intravenous line stopcock	A sterile valve that is typically a component of an intravenous (IV) administration set and designed to be manually-operated by healthcare staff to regulate the flow of intravenous solution delivered to a patient. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FPA	Set, administration, intravascular
FMG	Stopcock, i.V. Set

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K130245	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
No Device Sizes

Device Record Status

Public Device Record Key: ab880ac4-04e1-46fa-b74b-bff89679ac97
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: September 24, 2016