| Primary Device ID | 14953170309134 |
| NIH Device Record Key | 7170937c-a920-449e-9732-1c62b45e1ebd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Single Use Aspiration Needle NA-220H/230H |
| Version Model Number | NA-220H-8022 |
| Company DUNS | 711789789 |
| Company Name | OLYMPUS MEDICAL SYSTEMS CORP. |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx | |
| Phone | +1(800)401-1086 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04953170309137 [Primary] |
| GS1 | 14953170309134 [Package] Contains: 04953170309137 Package: [5 Units] In Commercial Distribution |
| FCG | Biopsy needle |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-21 |
| 14953170309233 | NA-230H-8022 |
| 14953170309219 | Single Use Aspiration Needle NA-220H/230H |
| 14953170309158 | NA-220H-8022 |
| 14953170309134 | Single Use Aspiration Needle NA-220H/230H |
| 14953170309110 | NA-220H-8019 |
| 14953170309097 | Single Use Aspiration Needle NA-220H/230H |