Primary Device ID | 00817770020677 |
NIH Device Record Key | fccca43f-7f28-4c7e-95e0-c222c47f9d25 |
Commercial Distribution Discontinuation | 2019-05-06 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | MAXO2+ |
Version Model Number | R217P62-004 |
Company DUNS | 169911828 |
Company Name | MAXTEC, LLC |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817770020677 [Primary] |
CCL | Analyzer, Gas, Oxygen, Gaseous-Phase |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-05-07 |
Device Publish Date | 2016-09-26 |
00817770020967 | Analyzer with MicroMax BlenderBuddy 0-15 0-3.5 |
00817770020950 | Analyzer with MicroMax BlenderBuddy 0-70 DISS |
00817770020943 | Analyzer with Optiflow Jr. |
00817770020677 | MaxO2+A Analyzer with Adapter |
00817770020660 | Medical A International Analyzer |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MAXO2+ 78340964 3069090 Live/Registered |
MAXTEC, LLC 2003-12-15 |