| Primary Device ID | 04038917411820 |
| NIH Device Record Key | 4a129529-e2e1-4ff0-b81c-0ca5cea9b0fc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Biosphere® Screw Cap, blue |
| Version Model Number | 65.716.221 |
| Catalog Number | 65.716.221 |
| Company DUNS | 388000270 |
| Company Name | Sarstedt Aktiengesellschaft & Co.KG |
| Device Count | 50 |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04038917411813 [Primary] |
| GS1 | 04038917411820 [Unit of Use] |
| KDT | Container, Specimen Mailer And Storage, Sterile |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-08-04 |
| Device Publish Date | 2025-07-25 |
| 04038917277730 | 65.716.201 |
| 04038917411820 | 65.716.221 |