Primary Device ID | 04260277176723 |
NIH Device Record Key | 6f7651c9-187e-418c-bc22-f270da0f2af0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Disposable Semi-Automatic Biopsy Gun |
Version Model Number | SBG-2010-18-0200 |
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 | 04260277176525 [Primary] |
GS1 | 04260277176723 [Package] Contains: 04260277176525 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 |
04260277176792 | SBG-2010-20-0300 |
04260277176785 | SBG-2010-20-0250 |
04260277176778 | SBG-2010-20-0200 |
04260277176761 | SBG-2010-20-0150 |
04260277176754 | SBG-2010-20-0100 |
04260277176747 | SBG-2010-18-0300 |
04260277176730 | SBG-2010-18-0250 |
04260277176723 | SBG-2010-18-0200 |
04260277176716 | SBG-2010-18-0150 |
04260277176709 | SBG-2010-18-0100 |
04260277176693 | SBG-2010-16-0300 |
04260277176686 | SBG-2010-16-0250 |
04260277176679 | SBG-2010-16-0200 |
04260277176662 | SBG-2010-16-0150 |
04260277176655 | SBG-2010-16-0100 |
04260277176648 | SBG-2010-14-0300 |
04260277176631 | SBG-2010-14-0250 |
04260277176624 | SBG-2010-14-0200 |
04260277176617 | SBG-2010-14-0150 |
04260277176600 | SBG-2010-14-0100 |