Primary Device ID | 00859806007030 |
NIH Device Record Key | 6b407924-ad73-46f6-b78b-ddd9b4af57a4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Clarifi Cart |
Version Model Number | 085980600703 |
Company DUNS | 603130928 |
Company Name | MODULATED IMAGING INC. |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
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 | 00859806007030 [Primary] |
MUD | Oximeter, Tissue Saturation |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-04-19 |
Device Publish Date | 2019-04-03 |
00859806007016 - Ox-Imager | 2020-07-01 The Ox-Imager CS™ is intended for use by healthcare professionals as a noninvasive tissue oxygenation measurement system that |
00859806007030 - Clarifi Cart | 2019-04-19Cart |
00859806007030 - Clarifi Cart | 2019-04-19 Cart |
00859806007023 - Clarifi Imaging System | 2019-04-19 Tissue Saturation Oximeter |