| Primary Device ID | 04719880180493 |
| NIH Device Record Key | c0d4259e-552c-47e4-ab54-f0853e35040e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Haritex Corporation |
| Version Model Number | HC-43 |
| Catalog Number | HC-43 |
| Company DUNS | 656398765 |
| Company Name | HARITEX CORPORATION |
| Device Count | 125 |
| 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 | false |
| 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 | 04719880180486 [Unit of Use] |
| GS1 | 04719880180493 [Primary] |
| GS1 | 14719880180490 [Package] Package: [4 Units] In Commercial Distribution |
| GDT | Staple, Removable (Skin) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-27 |
| Device Publish Date | 2023-06-19 |
| 04719880180493 | Staple Remover(Skin) plastic handles |
| 04719880180523 | Thumb Forceps, 5" Single Use. |
| 04719880180431 | Wire Scissors, Sharp/Sharp, 12 pieces/PE bag |
| 04719880180349 | Thumb Forceps, 4" Single Use. |
| 14719880180513 | FORCEPS WIRE HEMO KELLY STR 5-1/2", SINGLE USE. |
| 14719880180544 | Thumb forceps, 5", single use. Zi |