| Primary Device ID | 04038917418874 |
| NIH Device Record Key | c3c452ac-2677-4da0-99a8-2f6943d1f975 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Adapter sleeve |
| Version Model Number | 14.1216 |
| 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 | 04038917418867 [Primary] |
| GS1 | 04038917418874 [Unit of Use] |
| JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-06 |
| Device Publish Date | 2024-04-26 |
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