Primary Device ID | 00816389023451 |
NIH Device Record Key | 860fce13-dc65-4cce-b531-ea9f805d0650 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Front segment, 25 mm diameter, distal source position |
Version Model Number | GM11005080 |
Catalog Number | GM11005080 |
Company DUNS | 332474605 |
Company Name | Varian Medical Systems Deutschland GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Outer Diameter | 25 Millimeter |
Outer Diameter | 25 Millimeter |
Outer Diameter | 25 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816389023451 [Primary] |
JAQ | System, applicator, radionuclide, remote-controlled |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00816389023451]
Moist Heat or Steam Sterilization
[00816389023451]
Moist Heat or Steam Sterilization
[00816389023451]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-22 |