Colpostat segment, 30mm diameter for Fletcher Applicator Set GM11001120

GUDID 00816389021891

VARIAN MEDICAL SYSTEMS, INC.

Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading
Primary Device ID00816389021891
NIH Device Record Keydcb2461d-84ce-4ffa-aade-3b84fb0e8bfa
Commercial Distribution StatusIn Commercial Distribution
Brand NameColpostat segment, 30mm diameter for Fletcher Applicator Set
Version Model NumberGM11001120
Catalog NumberGM11001120
Company DUNS009120817
Company NameVARIAN MEDICAL SYSTEMS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100816389021891 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JAQSystem, applicator, radionuclide, remote-controlled

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


[00816389021891]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-02-10
Device Publish Date2021-02-02

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