| Primary Device ID | 07611969952144 |
| NIH Device Record Key | 8bb788dc-3fc0-4db5-b090-dda1b8582e29 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IH-Card Rh-Phenotype+K |
| Version Model Number | 813201100 |
| Catalog Number | 813201100 |
| 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 | 07611969952144 [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 |
| 07611969964642 | Blood Grouping Reagent; Gel card for use with the IH-system; Card for Rh-Phenotype and Kell typi |
| 07611969964635 | Blood Grouping Reagent; Gel card for use with the IH-system; Card for Rh-Phenotype and Kell typi |
| 07611969952144 | Blood Grouping Reagent; Gel card for use with the IH-system; Card for Rh-Phenotype and Kell typi |