| Primary Device ID | 04046955207114 |
| NIH Device Record Key | aebc7512-fa08-410c-8e2c-5bd1f2407468 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DSM |
| Version Model Number | PV012SU |
| Catalog Number | PV012SU |
| Company DUNS | 315018218 |
| Company Name | Aesculap AG |
| Device Count | 5 |
| DM Exempt | false |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04046955207114 [Unit of Use] |
| GS1 | 04046955207121 [Primary] |
| PUI | Drape, surgical, exempt |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-07-01 |
| Device Publish Date | 2020-05-04 |
| 04046955207114 | STERILE DRAPE |
| 04046955206766 | FOOT SWITCH WIRELESS |