| Primary Device ID | 00868906000100 |
| NIH Device Record Key | 9368f0cd-a038-444b-9305-a96944a294d6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GenUltimate! |
| Version Model Number | 100-50 |
| Catalog Number | 100-50 |
| Company DUNS | 829145387 |
| Company Name | PHARMA TECH SOLUTIONS, INC. |
| Device Count | 50 |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Phone | 805-446-2973 |
| intermania@aol.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00868906000100 [Primary] |
| GS1 | 00868906000131 [Unit of Use] |
| GS1 | 10868906000107 [Package] Package: Inner Pack [24 Units] In Commercial Distribution |
| GS1 | 10868906000121 [Package] Contains: 10868906000107 Package: Case [18 Units] In Commercial Distribution |
| CGA | Glucose Oxidase, Glucose |
| 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 | 2016-09-01 |
| 00868906000100 | Value Priced Test Strips for use with OneTouch®Ultra®, OneTouch® Ultra®2 and OneTouch® Ultr |
| 00867396000324 | Value Priced Test Strips for use with OneTouch®Ultra®, OneTouch® Ultra®2 and OneTouch® Ultr |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() GENULTIMATE! 86656415 5004741 Live/Registered |
PharmaTech Solutions, Inc. 2015-06-09 |