| Primary Device ID | 04260277175047 |
| NIH Device Record Key | 52109344-032a-4aeb-9c87-bf76dce66e91 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fullcore Biopsy Needle |
| Version Model Number | DNG-2020-16-0150 |
| 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 | 04260277175009 [Primary] |
| GS1 | 04260277175047 [Package] Contains: 04260277175009 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 |
| 04260277178109 | DNG-2020-18-0250 |
| 04260277178086 | DNG-2020-16-0250 |
| 04260277175061 | DNG-2020-16-0200 |
| 04260277175054 | DNG-2020-16-0160 |
| 04260277175047 | DNG-2020-16-0150 |
| 04260277175030 | DNG-2020-16-0100 |
| 04260277174767 | DNG-2020-18-0200 |
| 04260277174750 | DNG-2020-18-0160 |
| 04260277174743 | DNG-2020-18-0100 |
| 04260277174705 | DNG-2020-14-0200 |
| 04260277174699 | DNG-2020-14-0160 |
| 04260277174651 | DNG-2020-14-0100 |