Pair of titanium colpostat probes (left & right) GM11010700

GUDID 00810563022353

Varian Medical Systems Deutschland GmbH

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 Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading
Primary Device ID00810563022353
NIH Device Record Keyd9e8037e-b6a5-4d02-aacb-7b95e0ebd89a
Commercial Distribution StatusIn Commercial Distribution
Brand NamePair of titanium colpostat probes (left & right)
Version Model NumberGM11010700
Catalog NumberGM11010700
Company DUNS332474605
Company NameVarian Medical Systems Deutschland GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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
GS100810563022353 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JAQSystem, applicator, radionuclide, remote-controlled

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


[00810563022353]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-11
Device Publish Date2023-10-03

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10816389020334 - Transfer Guide Tube + for 200 mm catheters2024-02-28
00816389020344 - Transfer Guide Tube + for 250 mm catheters2024-02-28
10816389020358 - Transfer Guide Tube + of 500 mm length for catheters2024-02-28
20816389020362 - Transfer Guide Tube + of 1000 mm length for catheters2024-02-28
10816389020372 - Transfer Guide Tube + of 1000 mm length for Luer connections2024-02-28

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