| Primary Device ID | 00827002176393 | 
| NIH Device Record Key | 2fa7004e-a9d1-4d68-ae82-7684591b94d5 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Dretler | 
| Version Model Number | G17639 | 
| Catalog Number | 025505-GRAD | 
| Company DUNS | 042823948 | 
| Company Name | COOK INCORPORATED | 
| 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(812)330-5494 | 
| sharedservices@cookmedical.com | 
| Special Storage Condition, Specify | Between 0 and 0 *Store in dark, dry, cool place. | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00827002176393 [Primary] | 
| LJE | CATHETER, NEPHROSTOMY | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2020-03-19 | 
| Device Publish Date | 2016-09-24 | 
| 00827002151680 | Dretler Ureteroscopy Stent Set | 
| 00827002151109 | Dretler Ureteroscopy Stent Set | 
| 00827002145146 | Dretler Ureteroscopy Stent Set | 
| 00827002178137 | Dretler Ureteroscopy Stent Set | 
| 00827002176393 | Dretler Ureteroscopy Stent Set | 
| 00827002157354 | Dretler Ureteroscopy Stent Set |