| Primary Device ID | 05032384013203 |
| NIH Device Record Key | f941d460-bf96-492c-8580-8051f83ed39d |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | DR0801M |
| Company DUNS | 365355452 |
| Company Name | OXOID LIMITED |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +441256694238 |
| oxoid.techsupport@thermofisher | |
| Phone | +441256694238 |
| oxoid.techsupport@thermofisher.com | |
| Phone | +441256694238 |
| oxoid.techsupport@thermofisher.com | |
| Phone | +441256694238 |
| oxoid.techsupport@thermofisher.com | |
| Phone | +441256694238 |
| oxoid.techsupport@thermofisher.com | |
| Phone | +441256694238 |
| oxoid.techsupport@thermofisher.com | |
| Phone | +441256694238 |
| oxoid.techsupport@thermofisher.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05032384013203 [Primary] |
| MJH | Legionella, Spp., Elisa |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-24 |