Primary Device ID | 20681490008529 |
NIH Device Record Key | c70d5e9e-ae70-4949-b6a9-506a45be2487 |
Commercial Distribution Discontinuation | 2017-11-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Affinity® |
Version Model Number | CB351 |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, INC. |
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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Pore Size | 38 Micrometer |
Pore Size | 38 Micrometer |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00681490008525 [Primary] |
GS1 | 20681490008529 [Package] Contains: 00681490008525 Package: PK [6 Units] Discontinued: 2017-11-30 Not in Commercial Distribution |
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 | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-06-16 |
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50613994011249 | FILTER 61399401124 AFFINITY 6CA ART 351 |
00643169778177 | PROBE ATP210 AFFINITY TEMPERATURE |
20643169178124 | FILTER BB851 AF100 WITH BALANCE |
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20681490008574 | OXYGENATOR CB511 AFFINITY BIOACT |
20681490008536 | FILETR CB353 BIOAC 20M AFFINITY |
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20681490008024 | FILTER 61399409503 AFFINITY ART 354 6PK |
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