| Primary Device ID | 04038917167079 |
| NIH Device Record Key | 33deec14-5771-4896-a508-21e03c88bd64 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tube-Segment-Opener |
| Version Model Number | 95.1000 |
| Catalog Number | 95.1000 |
| 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 | 04038917084949 [Primary] |
| GS1 | 04038917167079 [Unit of Use] |
| LXG | EQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-12-08 |
| Device Publish Date | 2022-11-30 |
| 04038917199056 | 95.1000.800 |
| 04038917167079 | 95.1000 |