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 |