| Primary Device ID | 00887761968455 |
| NIH Device Record Key | 94f39622-ed0c-4a51-9594-30218c7fe5a9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VidiaPort |
| Version Model Number | 4028310 |
| 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 | 00887761968455 [Primary] |
| KQM | CAMERA, SURGICAL AND ACCESSORIES |
| 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 |
| 00887761968523 | VidiaPort Ceiling Single |
| 00887761968462 | VidiaPort Ceiling Duo |
| 00887761968455 | VidiaPort Ceiling Trio |