Primary Device ID | 04260277173203 |
NIH Device Record Key | de47e3cf-e306-4d96-9968-df16ed327508 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bone marrow biopsy system |
Version Model Number | BOW-1060-11-0150 |
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 | 04260277173166 [Primary] |
GS1 | 04260277173203 [Package] Contains: 04260277173166 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 |
04260277175832 | BOW-1070-15-0041 |
04260277173203 | BOW-1060-11-0150 |
04260277173197 | BOW-1060-11-0100 |
04260277173180 | BOW-1060-08-0150 |
04260277173135 | BOW-1060-08-0100 |
04260632793367 | BOW-1066-13-0100 |
04260632793350 | BOW-1066-13-0062 |
04260632793343 | BOW-1066-11-0150 |
04260632793336 | BOW-1066-11-0125 |
04260632793329 | BOW-1066-11-0100 |
04260632793312 | BOW-1066-08-0150 |
04260632793305 | BOW-1066-08-0125 |
04260632793213 | BOW-1066-08-0100 |
04260632793206 | BOW-1076-15-0100 |
04260632793190 | BOW-1076-15-0050 |