| Primary Device ID | 05056080501659 |
| NIH Device Record Key | 6fb9f565-d948-45bc-b40f-035a6df3b8d7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sample Collection Tubes |
| Version Model Number | R30853001 |
| Company DUNS | 232600853 |
| Company Name | REMEL EUROPE 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05056080501659 [Primary] |
| LIB | Device, General Purpose, Microbiology, Diagnostic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-07-29 |
| Device Publish Date | 2021-07-21 |