| Primary Device ID | 00850041090917 |
| NIH Device Record Key | 79d936fd-364a-4b82-868f-97ed61cdf85b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MULTICHEM |
| Version Model Number | 2010-0260 |
| Company DUNS | 106267123 |
| Company Name | Lgc Clinical Diagnostics, 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 | true |
| Device Combination Product | false |
| Single Use | false |
| 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 | 00850041090917 [Primary] |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-05-23 |
| Device Publish Date | 2025-05-15 |
| 00850041090917 | 2010-0260 |
| 00850041090900 | 2015-0337 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MULTICHEM 85830464 not registered Dead/Abandoned |
Techno-Path (Distribution) 2013-01-23 |
![]() MULTICHEM 75692778 2395185 Dead/Cancelled |
Stowe Woodward LLC 1999-04-28 |
![]() MULTICHEM 75119280 not registered Dead/Abandoned |
MultiChem Analytical Services, L.L.C. 1996-06-14 |
![]() MULTICHEM 74264775 1748157 Dead/Cancelled |
NALCO/EXXON ENERGY CHEMICALS, L.P. 1992-04-13 |
![]() MULTICHEM 74241188 1721946 Live/Registered |
PURETEC CORPORATION 1992-01-29 |
![]() MULTICHEM 72188992 0782398 Dead/Expired |
MILTON ROY COMPANY 1964-03-18 |