| Primary Device ID | 08056646504787 |
| NIH Device Record Key | f385728e-3081-4d54-90b5-3950d356101c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Punches, NOBEL |
| Version Model Number | 32.Z2002.00 |
| Company DUNS | 447696675 |
| Company Name | OMNIA SRL |
| 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 | true |
| 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 | 08056646504787 [Unit of Use] |
| GS1 | 08056646504794 [Primary] |
| EME | Punch, Biopsy, Surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-08-17 |
| Device Publish Date | 2021-08-09 |
| 08056646504862 | Guided Soft Tissue Punch 6.0/WP 5/pkg |
| 08056646504848 | Guided Soft Tissue Punch RP 5/pkg |
| 08056646504824 | Guided Soft Tissue Punch NP 5/pkg |
| 08056646504800 | Soft Tissue Punch Ø 6.2 mm, 5-pack |
| 08056646504787 | Soft Tissue Punch Ø 5.2 mm, 5-pack |
| 08056646504763 | Soft Tissue Punch Ø 4.1 mm, 5-pack |