| Primary Device ID | 20705032056127 |
| NIH Device Record Key | 96d61a9e-8316-4467-b406-cf0e8f9a02c8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BIOPSY FORCEPS STD |
| Version Model Number | 504302L |
| Catalog Number | 504302L |
| Company DUNS | 806136177 |
| Company Name | CORDIS CORPORATION |
| 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 | false |
| 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 | 10705032056120 [Primary] |
| GS1 | 20705032056127 [Package] Contains: 10705032056120 Package: Box [1 Units] In Commercial Distribution |
| DWZ | DEVICE, BIOPSY, ENDOMYOCARDIAL |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-03-04 |
| Device Publish Date | 2024-02-23 |
| 20705032055212 - EMERALD | 2024-08-08 EMERALD GUIDEWIRES (OEM) |
| 20705032057407 - Palmaz Genesis | 2024-08-08 STENT GENESIS 12MM PERIPHERAL |
| 20705032057445 - Palmaz Genesis | 2024-08-08 STENT GENESIS 18MM PERIPHERAL |
| 20705032057537 - Palmaz Genesis | 2024-08-08 STENT GENESIS 29MM PERIPHERAL |
| 20705032057575 - Palmaz Genesis | 2024-08-08 STENT GENESIS 39MM PERIPHERAL |
| 20705032057612 - Palmaz Genesis | 2024-08-08 STENT GENESIS 59MM PERIPHERAL |
| 20705032062029 - PALMAZ BLUE | 2024-08-08 Blue/AviatorPlus 5x12/80P PKG |
| 20705032062258 - PALMAZ BLUE | 2024-08-08 Blue/AviatorPlus 5x24/80P PKG |