Primary Device ID | EPTWTM600170 |
NIH Device Record Key | 235566df-b728-4953-9711-736688e94108 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | Dosimetry Diode E |
Catalog Number | TM60017 |
Company DUNS | 318749751 |
Company Name | PTW-Freiburg Physikalisch-Technische Werkstätten Dr. Pychlau GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | EPTWTM600170 [Primary] |
IYE | Accelerator, Linear, Medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-04-27 |
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EPTWT100580 - OCTAVIUS | 2023-12-07 |
EPTWS0700160 - NA | 2018-07-06 |
EPTWS1000090 - NA | 2018-07-06 |
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EPTWT100060 - NA | 2018-07-06 |