| Primary Device ID | 00810024670284 |
| NIH Device Record Key | decb77f6-44b2-4697-9929-14e252b7891e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LUKE BX Single Use Biopsy Forceps |
| Version Model Number | BFC-MD-000650 |
| Company DUNS | 117126091 |
| Company Name | CENTERPOINT SYSTEMS LLC |
| Device Count | 1 |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810024670284 [Primary] |
| FCL | Forceps, Biopsy, Non-Electric |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-07-30 |
| Device Publish Date | 2024-07-22 |
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