| Primary Device ID | 20353885011802 |
| NIH Device Record Key | 114579ae-8a2f-48f2-8f8f-fa5a1caec1a8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OneTouch Verio Blood Glucose Monitoring System. |
| Version Model Number | 024041 |
| Catalog Number | 02404101 |
| Company DUNS | 480240820 |
| Company Name | LifeScan Europe GmbH |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Phone | 8885673003 |
| XX@XX.XX |
| Needle Gauge | 30 Gauge |
| Storage Environment Temperature | Between 41 Degrees Fahrenheit and 86 Degrees Fahrenheit |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00353885011808 [Primary] |
| GS1 | 20353885011802 [Package] Contains: 00353885011808 Package: shipper case [4 Units] In Commercial Distribution |
| NDC/NHRIC | 53885-041-01 [Secondary] |
| NBW | System, Test, Blood Glucose, Over The Counter |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-03-21 |
| Device Publish Date | 2019-03-13 |
| 20353885011819 | OneTouch Verio Blood Glucose Monitoring System. |
| 20353885011802 | OneTouch Verio Blood Glucose Monitoring System. |