Primary Device ID | 00854003008019 |
NIH Device Record Key | 566fa29e-0283-4094-8b19-4b1bacb220a1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sensica |
Version Model Number | SSPK-1001 |
Company DUNS | 090250920 |
Company Name | ADAPTEC MEDICAL DEVICES 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 | true |
Expiration Date | false |
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 | 00854003008019 [Primary] |
EXS | Urinometer, Electrical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-09-13 |
Device Publish Date | 2019-09-05 |
00854003008019 - Sensica | 2019-09-13 |
00854003008019 - Sensica | 2019-09-13 |
10854003008009 - Sensica UO | 2018-11-30 Automated urine meter system for continuous monitoring of urine output |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SENSICA 87007617 5476096 Live/Registered |
Adaptec Medical Devices 2016-04-20 |
SENSICA 86072602 4635510 Live/Registered |
Derma Dream Group Ltd. 2013-09-24 |