AccessGUDID - DEVICE: Cleaning caps, black (pack of 20) (interstitial tube connector) (10816389027166)

GUDID

Device Identifier (DI) Information

Brand Name: Cleaning caps, black (pack of 20) (interstitial tube connector)
Version or Model: GM11003360
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: VARIAN MEDICAL SYSTEMS, INC.

Primary DI Number: 10816389027166
Issuing Agency: GS1
Commercial Distribution End Date: February 29, 2020
Device Count: 20
Labeler D-U-N-S® Number*: 009120817 *Terms of Use

Device Description: No description.

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:	No
Prescription Use (Rx):	No
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?
38437	Brachytherapy system remote afterloading source transfer tube	A tube or hose-like catheter with connectors at both ends used to interface the brachytherapy applicator to the remote afterloading system. The transfer tube, when attached to the applicator and the afterloading system, provides a continuous closed passage that allows for moving either a radioactive source(s) and/or positioning markers from the shielded source storage compartment of the remote afterloading brachytherapy system into appropriate positions within a brachytherapy applicator that has been positioned at a location either on the surface of, or within, the patient.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JAQ	System, applicator, radionuclide, remote-controlled

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K141336	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
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: a25048d4-5ab6-464f-a529-445fcc3f2223
Public Version Date: June 11, 2020
Public Version Number: 4
DI Record Publish Date: September 19, 2016