| Primary Device ID | 00816611021132 |
| NIH Device Record Key | 3f7d1731-e1e1-4169-b217-aaccb9082225 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AngioSystems Drape |
| Version Model Number | 060-1722A |
| Company DUNS | 144884467 |
| Company Name | ANGIOSYSTEMS, INCORPORATED |
| Device Count | 250 |
| 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 | 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 | 00816611020388 [Unit of Use] |
| GS1 | 00816611021132 [Primary] |
| KKX | Drape, Surgical |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00816611021132]
Ethylene Oxide
[00816611021132]
Ethylene Oxide
[00816611021132]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-06-15 |