| Primary Device ID | H862NCP0835HB2 |
| NIH Device Record Key | 3c60580a-a3a7-42e0-bb45-2d7361d35aaa |
| Commercial Distribution Discontinuation | 2018-04-25 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Nephro-Cath Nephrostomy Drainage Catheter |
| Version Model Number | NCP-0835HB |
| Catalog Number | NCP-0835HB |
| Company DUNS | 192559557 |
| Company Name | URESIL, LLC |
| Device Count | 1 |
| 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 | 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 | 1-800-538-7374 |
| sales@uresil.com |
| Length | 29 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | H862NCP0835HB0 [Primary] |
| HIBCC | H862NCP0835HB1 [Package] Contains: H862NCP0835HB0 Package: Dispenser [5 Units] Discontinued: 2018-04-25 Not in Commercial Distribution |
| HIBCC | H862NCP0835HB2 [Package] Contains: H862NCP0835HB1 Package: Shipper [4 Units] Discontinued: 2018-04-25 Not in Commercial Distribution |
| GBO | Catheter, Nephrostomy, General & Plastic Surgery |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-01-28 |
| Device Publish Date | 2016-09-06 |
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