| Primary Device ID | 04038917194082 |
| NIH Device Record Key | 2a8a2522-a7a9-416a-ba66-23503ea63ef4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Screw cap, neutral |
| Version Model Number | 65.716.725 |
| Catalog Number | 65.716.725 |
| Company DUNS | 388000270 |
| Company Name | Sarstedt Aktiengesellschaft & Co.KG |
| Device Count | 500 |
| DM Exempt | true |
| 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 |
| Phone | +1(800)257-5101 |
| customerservice.us@sarstedt.com | |
| Phone | +1(800)257-5101 |
| customerservice.us@sarstedt.com | |
| Phone | +1(800)257-5101 |
| customerservice.us@sarstedt.com | |
| Phone | +1(800)257-5101 |
| customerservice.us@sarstedt.com | |
| Phone | +1(800)257-5101 |
| customerservice.us@sarstedt.com | |
| Phone | +1(800)257-5101 |
| customerservice.us@sarstedt.com | |
| Phone | +1(800)257-5101 |
| customerservice.us@sarstedt.com | |
| Phone | +1(800)257-5101 |
| customerservice.us@sarstedt.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04038917118989 [Primary] |
| GS1 | 04038917194082 [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 | 2022-12-08 |
| Device Publish Date | 2022-11-30 |
| 04038917308250 | 65.163.002 |
| 04038917272230 | 65.163 |
| 04038917194082 | 65.716.725 |
| 04038917166386 | 65.805 |
| 04038917165860 | 65.716 |
| 04038917165839 | 65.712 |