| Primary Device ID | 50653160021382 |
| NIH Device Record Key | cb8007ce-3b30-4f96-9691-bdca0963d530 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Centurion |
| Version Model Number | CS200 |
| Company DUNS | 017246562 |
| Company Name | CENTURION MEDICAL PRODUCTS CORPORATION |
| Device Count | 1 |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)248-4058 |
| CUSTOMERSERVICE@CENTURIONMP.COM | |
| Phone | +1(800)248-4058 |
| CUSTOMERSERVICE@CENTURIONMP.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00653160021387 [Primary] |
| GS1 | 50653160021382 [Package] Contains: 00653160021387 Package: CASE [200 Units] In Commercial Distribution |
| HFW | Clamp, umbilical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-03-03 |