| Primary Device ID | 20886333206852 |
| NIH Device Record Key | 01c456e6-f721-4a3c-91c8-8d2590576718 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Jawz Endomyocardial Biopsy Forcep |
| Version Model Number | 190090 |
| Catalog Number | 190090 |
| Company DUNS | 140727624 |
| Company Name | ARGON MEDICAL DEVICES, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 |
| Phone | 1.800.927.4669 |
| Customer.Service@argonmedical.com | |
| Phone | 1.800.927.4669 |
| Customer.Service@argonmedical.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00886333206858 [Primary] |
| GS1 | 20886333206852 [Package] Contains: 00886333206858 Package: Box [10 Units] In Commercial Distribution |
| DWZ | Device, Biopsy, Endomyocardial |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-09-10 |
| Device Publish Date | 2016-09-16 |
| 20886333206869 | Jawz Endomyocardial Biopsy Forceps 5F x 105cm Straight |
| 20886333206852 | Jawz Endomyocardial Biopsy Forceps 5F x 50cm Straight |
| 20886333206777 | Jawz Endomyocardial Biopsy Forceps 6F x 50cm Straight |