| Primary Device ID | 00384701402036 |
| NIH Device Record Key | f6f9418a-bce7-4df1-ac3c-a4739b8012b4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Unistik Touch |
| Version Model Number | AT 1402 |
| Company DUNS | 217266915 |
| Company Name | OWEN MUMFORD LIMITED |
| Device Count | 100 |
| 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 | 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 | true |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Needle Gauge | 23 Gauge |
| Depth | 2 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00384701402005 [Unit of Use] |
| GS1 | 00384701402012 [Primary] |
| GS1 | 00384701402036 [Package] Contains: 00384701402012 Package: Case [40 Units] In Commercial Distribution |
| FMK | Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-04-07 |
| Device Publish Date | 2023-03-30 |
| 00384701402036 - Unistik Touch | 2023-04-07Unistik Touch contact activated safety lancets - 23G x 2.0mm - medium flow |
| 00384701402036 - Unistik Touch | 2023-04-07 Unistik Touch contact activated safety lancets - 23G x 2.0mm - medium flow |
| 00384701015038 - Unistik | 2023-02-15 Unistik Safety Lancet Economy - 21G |
| 00384701027024 - Unistik 3 | 2023-02-15 Unistik 3 Safety Lancet Gentle - 30G |
| 00384701614033 - Unistik Pro | 2023-02-15 Unistik Pro Safety Lancet - 21G x 2.0mm |
| 00384701634031 - Unistik Pro | 2023-02-15 Unistik Pro Safety Lancet - 25G x 1.6mm |
| 00384701644030 - Unistik Pro | 2023-02-15 Unistik Pro Safety Lancet - 28G x 1.2mm |
| 00384701404030 - Unistik Touch - Contact Activated Safety Lancet - 23G x 2.0mm | 2021-04-12 Sterile, single use safety lancet |
| 00384701412035 - Unistik Touch - Contact Activated Safety Lancet - 21G x 2.0mm | 2021-04-12 Sterile, single use safety lancet |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() UNISTIK TOUCH 86709277 5020498 Live/Registered |
Owen Mumford Limited 2015-07-30 |