Primary Device ID | 04260277175054 |
NIH Device Record Key | 50bb1b0f-b2fb-4579-bea1-1b707a94ba8a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fullcore Biopsy Needle |
Version Model Number | DNG-2020-16-0160 |
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 | 04260277175016 [Primary] |
GS1 | 04260277175054 [Package] Contains: 04260277175016 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 |