Primary Device ID | 04037691739335 |
NIH Device Record Key | 51fe94cf-665c-4097-8a8a-c310a816c7f2 |
Commercial Distribution Discontinuation | 2020-02-01 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | QUADROX-iD |
Version Model Number | BEQ-01970311 |
Catalog Number | 70105.3325 |
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 | true |
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 |
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04058863019000 | QUADROX-iD Adult Diffusion Membrane Oxygenator, without Filter, NON-COATED, with a screw connec |
04037691741161 | QUADROX-iD Adult, without filter, SOFTLINE coating, non-sterilized, semi-finished Product. |
04037691739335 | QUADROX-iD Adult, without filter, BIOLINE Coating, non-sterile, semi-finished product. |
04058863299983 | QUADROX-iD Pediatric with BIOLINE Coating |
04037691576640 | 016061 Holder arm |