Primary Device ID | EPTWT100230 |
NIH Device Record Key | 95e30367-f60c-4f11-b37e-8db3f2d639ef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | UNIDOS webline |
Version Model Number | UNIDOS webline |
Catalog Number | T10023 |
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 | EPTWT100230 [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 | 2017-04-26 |
EPTWT100230 | UNIDOS webline |
EPTWT100220 | UNIDOS webline |
EPTWT100210 | UNIDOS webline |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
UNIDOS WEBLINE 85075212 3950300 Dead/Cancelled |
PTW NY Corporation 2010-06-30 |