| 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 |