Primary Device ID | 20816286021073 |
NIH Device Record Key | 34d6a193-3d00-4918-b471-faec2ab7a06b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BOEHRINGER® CareDry™ System |
Version Model Number | 7660 |
Company DUNS | 079991657 |
Company Name | BOEHRINGER LABORATORIES, 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10816286021076 [Primary] |
GS1 | 20816286021073 [Package] Contains: 10816286021076 Package: Box [20 Units] In Commercial Distribution |
NZU | Collector, Urine, Powered, Non Indwelling Catheter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-11-09 |
Device Publish Date | 2021-11-01 |
20816286021073 | CareDry™ System |
20816286021141 | CareDry™ System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BOEHRINGER 97186870 not registered Live/Pending |
Boehringer Laboratories, LLC 2021-12-23 |
BOEHRINGER 97186834 not registered Live/Pending |
Boehringer Laboratories, LLC 2021-12-23 |
BOEHRINGER 79167386 not registered Dead/Abandoned |
MAG IAS GmbH 2015-04-01 |
BOEHRINGER 79149890 4887150 Live/Registered |
MAG IAS GmbH 2014-03-27 |
BOEHRINGER 78300425 2934276 Dead/Cancelled |
Boehringer Ingelheim Pharma GmbH & Co. KG 2003-09-15 |
BOEHRINGER 77658159 3748503 Live/Registered |
Boehringer Laboratories, Inc. 2009-01-28 |
BOEHRINGER 72457895 1365035 Live/Registered |
BOEHRINGER, JOHN R. 1973-05-18 |