3D Interstitial Ring Applicator Set 60 degrees GM11010190

GUDID 00810563022230

Varian Medical Systems Deutschland GmbH

Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading Cervical/intrauterine brachytherapy system applicator, remote-afterloading
Primary Device ID00810563022230
NIH Device Record Key70730cdb-f8c3-4dc5-b339-ac5ace186c4c
Commercial Distribution StatusIn Commercial Distribution
Brand Name3D Interstitial Ring Applicator Set 60 degrees
Version Model NumberGM11010190
Catalog NumberGM11010190
Company DUNS332474605
Company NameVarian Medical Systems Deutschland GmbH
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 Datetrue
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
GS100810563022230 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JAQSystem, applicator, radionuclide, remote-controlled

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


[00810563022230]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-05-15
Device Publish Date2023-05-05

On-Brand Devices [3D Interstitial Ring Applicator Set 60 degrees]

00816389025226GM11010190
00810563022230GM11010190

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