Primary Device ID | 00887761974050 |
NIH Device Record Key | 28ad7109-2a9d-4049-bd73-601861d677da |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TS 7500 |
Version Model Number | 1854088 |
Company DUNS | 330961223 |
Company Name | TRUMPF Medizin Systeme GmbH + Co. KG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
OTC Over-The-Counter | false |
Phone | +4936715860 |
SURGICAL@HILLROM.COM | |
Phone | +4936715860 |
SURGICAL@HILLROM.COM | |
Phone | +4936715860 |
SURGICAL@HILLROM.COM | |
Phone | +4936715860 |
SURGICAL@HILLROM.COM | |
Phone | +4936715860 |
SURGICAL@HILLROM.COM | |
Phone | +4936715860 |
SURGICAL@HILLROM.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887761974050 [Primary] |
KXJ | Table, radiologic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-01-13 |
Device Publish Date | 2023-01-05 |
00887761974494 | Operating table top SQ14 X-TRA UT |
00887761974456 | OR table top Carbon FL U V |
00887761974340 | Operating table top PTS Combi Suite U |
00887761974326 | TruSystem 7500 Hybrid (MC) |
00887761974098 | OR table top Carbon X-TRA 7500 U V |
00887761974081 | TruSystem 7500 Hybrid (FC) |
00887761974074 | TruSystem 7500 Hybrid (SC) |
00887761974067 | TruSystem 7500 Hybrid Plus (FC) |
00887761974050 | TruSystem 7500 Hybrid Plus (SC) |