Primary Device ID | 04037691117911 |
NIH Device Record Key | 3f601ad2-b542-4c35-a427-9e88648fa02b |
Commercial Distribution Discontinuation | 2020-04-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | QUART |
Version Model Number | BO-HBF 140, SOFTLINE, Sterile |
Catalog Number | 70103.2033 |
Company DUNS | 316153865 |
Company Name | Maquet Cardiopulmonary AG |
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 |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com | |
Phone | +49072229320 |
info.cp@maquet.com |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Area/Surface Area | 570 Square centimeter |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Pore Size | 40 Micrometer |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04037691117911 [Package] Contains: 04037691253862 Package: [8 Units] Discontinued: 2020-04-30 Not in Commercial Distribution |
GS1 | 04037691253862 [Primary] |
DTM | Filter, blood, cardiopulmonary bypass, arterial line |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-04-30 |
Device Publish Date | 2017-03-13 |
04037691117911 | The QUART arterial filter (HBF 140) with SOFTLINE coating, sterile, is a screen filter with inte |
04037691173412 | QUART Arterial Filter with BIOLINE Coating, Sterile. The QUART arterial filter (HBF 140) is a sc |
04037691190402 | Quart Arterial Filter, no coating, HBF 140#Arterieller Filter Quart |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
QUART 76110531 2645155 Live/Registered |
MAQUET CARDIOPULMONARY GMBH 2000-08-16 |
QUART 74545650 1905499 Dead/Cancelled |
M.B. Quart Electronics U.S.A., Inc. 1994-07-05 |
QUART 74545649 not registered Dead/Abandoned |
M.B. Quart Electronics U.S.A., Inc. 1994-07-05 |
QUART 74540017 1913433 Dead/Cancelled |
M.B. Quart Electronics U.S.A., Inc. 1994-06-20 |
QUART 72359835 0922198 Dead/Expired |
DOUWE EGBERTS KONINKLIJKE TABAKSFABRIEK-KOFFIEBRANDERIJEN-THEEHANDEL N.V. 1970-05-15 |