| Primary Device ID | 04046768148345 |
| NIH Device Record Key | 501371a5-4c1d-4816-8189-ce01545d4474 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Extension plate |
| Version Model Number | 116033BC |
| Company DUNS | 315435859 |
| Company Name | MAQUET GmbH |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04046768148345 [Primary] |
| BWN | Table And Attachments, Operating-Room |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-29 |
| Device Publish Date | 2024-11-21 |
| 04046768138360 | 116032DC |
| 04046768137752 | N.A. |
| 04046768137745 | 116032BC |
| 04046768134638 | 116032FC |
| 04046768134621 | 116032AC |
| 04046768089037 | 113131FC |
| 04046768089013 | 113131BC |
| 04046768040922 | 118046A0 |
| 04046768031852 | 118032F0 |
| 04046768031838 | 118032A0 |
| 04046768000292 | 10035200 |
| 04046768150973 | 116033FC |
| 04046768148352 | 116033GC |
| 04046768148345 | 116033BC |
| 04046768148338 | 116033DC |