Primary Device ID | 00827002214484 |
NIH Device Record Key | c50b182a-0312-4953-86bd-5540725dafbe |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Huibregtse |
Version Model Number | G21448 |
Company DUNS | 988559035 |
Company Name | COOK IRELAND LTD |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00827002214484 [Primary] |
FGE | CATHETER, BILIARY, DIAGNOSTIC |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-10-24 |
00827002220201 | Huibregtse, Katon Pusher |
00827002214484 | Huibregtse, Guiding Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HUIBREGTSE 85723533 4328110 Live/Registered |
Cook Medical Technologies LLC 2012-09-07 |
HUIBREGTSE 74232970 1713394 Live/Registered |
COOK MEDICAL TECHNOLOGIES LLC 1991-12-23 |