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 |