| Primary Device ID | 07611969952113 |
| NIH Device Record Key | bf0c7eac-85b1-4ece-8e0c-44f27926bf4f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IH-Card Group A,B |
| Version Model Number | 813141100 |
| Catalog Number | 813141100 |
| Company DUNS | 312576506 |
| Company Name | Bio-Rad Medical Diagnostics GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 | 800-224-6723 |
| techsupport.bmd@bio-rad.com |
| Special Storage Condition, Specify | Between 0 and 0 *Upright position |
| Storage Environment Temperature | Between 18 Degrees Celsius and 25 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07611969952113 [Primary] |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-01-20 |
| 07611969964581 | Blood Grouping Reagent; Gel card for use with IH-system; Optional add on to standard ABO typing |
| 07611969964574 | Blood Grouping Reagent; Gel card for use with IH-system; Optional add on to standard ABO typing |
| 07611969952113 | Blood Grouping Reagent; Gel card for use with IH-system; Optional add on to standard ABO typing |