| Primary Device ID | 00810041632449 |
| NIH Device Record Key | 23b17eb9-cc38-48b3-ab03-78eedbf2f695 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Smith and Nephew |
| Version Model Number | EICA8875-01 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810041632449 [Primary] |
| GS1 | 10810041632446 [Package] Package: Box [1 Units] In Commercial Distribution |
| GS1 | 20810041632443 [Package] Contains: 10810041632446 Package: Case [24 Units] In Commercial Distribution |
| NUJ | Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2021-03-01 |
| Device Publish Date | 2019-12-13 |