BOEHRINGER® CareDry™ System
GUDID 20816286021073
CareDry™ System
BOEHRINGER LABORATORIES, LLC
Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use| 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 |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10816286021076 [Primary] |
| GS1 | 20816286021073 [Package] Contains: 10816286021076 Package: Box [20 Units] In Commercial Distribution |
FDA Product Code
| NZU | Collector, Urine, Powered, Non Indwelling Catheter |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-11-09 |
| Device Publish Date | 2021-11-01 |
On-Brand Devices [BOEHRINGER® CareDry™ System]
| 20816286021073 | CareDry™ System |
| 20816286021141 | CareDry™ System |
Trademark Results [BOEHRINGER]
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 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.