| Primary Device ID | 08800099904904 |
| NIH Device Record Key | bd3f92c4-56c9-49fb-b583-b3ad550d9d82 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Perfit ZR |
| Version Model Number | NU 22 D3 W |
| Company DUNS | 690045351 |
| Company Name | Vatechacucera, Inc. |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |