| Primary Device ID | 04260277173593 |
| NIH Device Record Key | fcb0800b-f5cd-4980-85b3-98353fdbd410 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Manual TruCut Biopsy Cannula |
| Version Model Number | MBY-1050-16-0152 |
| Company DUNS | 320405061 |
| Company Name | Möller Medical 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| 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 |
|---|---|
| GS1 | 04260277173432 [Primary] |
| GS1 | 04260277173593 [Package] Contains: 04260277173432 Package: [10 Units] In Commercial Distribution |
| KNW | Instrument, Biopsy |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-09-17 |
| Device Publish Date | 2018-08-17 |
| 04260277173647 | MBY-1050-14-0200 |
| 04260277173630 | MBY-1050-14-0152 |
| 04260277173623 | MBY-1050-14-0114 |
| 04260277173616 | MBY-1050-14-0075 |
| 04260277173609 | MBY-1050-16-0200 |
| 04260277173593 | MBY-1050-16-0152 |
| 04260277173586 | MBY-1050-16-0114 |
| 04260277173579 | MBY-1050-16-0075 |
| 04260277173562 | MBY-1050-17-0200 |
| 04260277173555 | MBY-1050-17-0152 |
| 04260277173548 | MBY-1050-17-0114 |
| 04260277173531 | MBY-1050-17-0075 |
| 04260277173524 | MBY-1050-18-0200 |
| 04260277173517 | MBY-1050-18-0152 |
| 04260277173500 | MBY-1050-18-0114 |
| 04260277173494 | MBY-1050-18-0075 |