| Primary Device ID | 04066916015398 |
| NIH Device Record Key | a87abef9-23ae-4c24-af07-73501ec26f0c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tube 10 ml 92 x 15 ml |
| Version Model Number | 62.610.202 |
| Company DUNS | 388000270 |
| Company Name | Sarstedt Aktiengesellschaft & Co.KG |
| Device Count | 100 |
| 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 | true |
| 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 | 04066916015398 [Unit of Use] |
| GS1 | 04066916015404 [Primary] |
| NNK | Container, Specimen Mailer And Storage, Non-Sterile |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-25 |
| Device Publish Date | 2024-12-17 |
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