Primary Device ID | 00812559011440 |
NIH Device Record Key | ec9326dd-6ab6-4011-b819-13b32baa3e42 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Quebec® Digital Darkfield Colony Counter |
Version Model Number | 13332700 |
Company DUNS | 126650253 |
Company Name | REICHERT, 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 | false |
Serial Number | true |
Manufacturing Date | true |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812559011440 [Primary] |
KZB | Automated Colony Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-08-20 |
Device Publish Date | 2025-08-12 |
00812559012485 - Ocu-Film® +" | 2025-08-25 |
00812559012492 - Ocu-Film® +" | 2025-08-22 |
00812559010238 - Ultramatic RX Master Phoropter | 2025-08-20 |
00812559010269 - Ultramatic RX Master Phoropter | 2025-08-20 |
00812559010290 - Illuminated Phoropter | 2025-08-20 |
00812559010320 - Illuminated Phoropter | 2025-08-20 |
00812559010559 - TF50 Trial Frame | 2025-08-20 |
00812559010566 - TS75 Trial Lens | 2025-08-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() QUEBEC 74718091 2038305 Live/Registered |
DREAMWELL, LTD. 1995-08-21 |
![]() QUEBEC 72395441 0941427 Dead/Expired |
ONEIDA LTD. 1971-06-21 |
![]() QUEBEC 72167599 0765063 Dead/Cancelled |
American Optical Company 1963-04-26 |