| Primary Device ID | 04719880180394 |
| NIH Device Record Key | daafb64d-440d-4766-acfb-f2983e340f7f |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | HC-42 |
| Company DUNS | 656398765 |
| Company Name | HARITEX CORPORATION |
| Device Count | 250 |
| 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 | 04719880180172 [Primary] |
| GS1 | 04719880180394 [Unit of Use] |
| GS1 | 14719880180179 [Package] Contains: 04719880180172 Package: Carton [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 | 2022-12-13 |
| Device Publish Date | 2022-12-05 |
| 14719880180544 - Haritex Corporation | 2023-08-29 Thumb forceps, 5", single use. Zi |
| 14719880180513 - Haritex Corporation | 2023-07-19 FORCEPS WIRE HEMO KELLY STR 5-1/2", SINGLE USE. |
| 04719880180349 - Haritex Corporation | 2023-06-27 Thumb Forceps, 4" Single Use. |
| 04719880180400 - NA | 2023-06-27 FORCEPS THUMB WIRE W/SERRATED INST. 5" SINGLE USE |
| 04719880180431 - Haritex Corporation | 2023-06-27 Wire Scissors, Sharp/Sharp, 12 pieces/PE bag |
| 04719880180523 - Haritex Corporation | 2023-06-27 Thumb Forceps, 5" Single Use. |
| 04719880180493 - Haritex Corporation | 2023-06-27 Staple Remover(Skin) plastic handles |
| 14719880180230 - NA | 2023-06-07 |