Primary Device ID | 10075537257897 |
NIH Device Record Key | ced6dc26-4409-4523-9a71-8f42b96fd4fc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Accu-Chek Safe-T-Pro |
Version Model Number | 03448622001 |
Catalog Number | 03448622001 |
Company DUNS | 141608724 |
Company Name | Roche Diagnostics Operations, Inc. |
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 | 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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00075537257890 [Primary] |
GS1 | 10075537257897 [Package] Contains: 00075537257890 Package: [6 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 | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-27 |
Device Publish Date | 2022-10-19 |
00365702702196 | Accu-Chek Safe-T-Pro Plus 5ct |
10365702702148 | Accu-Chek Safte-T-Pro Plus 200ct Coag 6/cs |
00365702700475 | Accu-Chek Safe-T-Pro Uno 10ct |
10365702700465 | Accu-Chek Safe-T-Pro Uno 200ct 16/cs |
10075537257897 | Accu-Chek Safe-T-Pro Plus 200ct |