| Primary Device ID | 00860239001328 |
| NIH Device Record Key | f348ea0e-aff5-4701-91b4-9cc0d03e93b4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kohli Catheter |
| Version Model Number | 20-100 |
| Catalog Number | 20-100 |
| Company DUNS | 094332961 |
| Company Name | NELLIE MEDICAL, LLC |
| 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 | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com | |
| Phone | 7758007300 |
| info@kohlicatheter.com |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Catheter Length | 440 Millimeter |
| Catheter Gauge | 16 French |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860239001304 [Primary] |
| GS1 | 00860239001311 [Package] Contains: 00860239001304 Package: Shelf Box [10 Units] In Commercial Distribution |
| GS1 | 00860239001328 [Package] Contains: 00860239001311 Package: Shipping Carton [10 Units] In Commercial Distribution |
| EZL | Catheter, Retention Type, Balloon |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-07-12 |
| Device Publish Date | 2019-07-02 |