| Primary Device ID | 00815137020285 |
| NIH Device Record Key | 6272f808-c54e-4164-9858-ffccfccb4c07 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pinnacle |
| Version Model Number | 330 |
| Company DUNS | 001157841 |
| Company Name | Beekley Corporation |
| Device Count | 12 |
| 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 | false |
| 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 | 00815137020285 [Primary] |
| GS1 | 10815137020282 [Unit of Use] |
| KGX | Tape And Bandage, Adhesive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2019-07-22 |
| 00815137021640 | Needle Localization Needle Protectors |
| 00815137020285 | Needle Localization Needle Protectors |