| Primary Device ID | 40301936721013 |
| NIH Device Record Key | d9305b3a-804c-48a5-882d-120b45874d91 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MICROLET®NEXT |
| Version Model Number | 6721 |
| Catalog Number | 85267302 |
| Company DUNS | 080028910 |
| Company Name | ASCENSIA DIABETES CARE US INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00301936721015 [Primary] |
| GS1 | 40301936721013 [Package] Contains: 00301936721015 Package: shipper/case [100 Units] In Commercial Distribution |
| FMK | Lancet, Blood |
| QRL | Multiple Use Blood Lancet For Single Patient Use Only |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-06-14 |
| Device Publish Date | 2019-06-06 |
| 40301936721013 | Alternative Site Testing (AST) Endcap |
| 40301936705013 | Lancing Device |
| 40301936702012 | Lancing Device. 1 Kit: 1 MICROLET®NEXT lancing device with adjustable endcap; 5 MICROLET® ste |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MICROLET 88151546 not registered Live/Pending |
Ascensia Diabetes Care Holdings AG 2018-10-11 |
![]() MICROLET 75069425 2100253 Dead/Cancelled |
BAYER CORPORATION 1996-03-08 |