| Primary Device ID | 08718734960966 |
| NIH Device Record Key | 79cde522-469b-4351-8979-34ee1d8812df |
| Commercial Distribution Discontinuation | 2024-08-28 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | HemoTrol WB |
| Version Model Number | High |
| Catalog Number | 08718734960966 |
| Company DUNS | 412925992 |
| Company Name | Eurotrol B.V. |
| 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 | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08718734960966 [Package] Contains: 08718734960997 Package: Box [2 Units] Discontinued: 2024-08-28 Not in Commercial Distribution |
| GS1 | 08718734960997 [Primary] |
| GGM | Control, Hemoglobin |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-08-29 |
| Device Publish Date | 2019-03-18 |
| 08718734960966 | HemoTrol® WB is an assayed quality control material for professional use to verify the performa |
| 08718734960959 | HemoTrol® WB is an assayed quality control material for professional use to verify the performa |
| 08718734960973 | HemoTrol® WB is an assayed quality control material for professional use to verify the performa |