Primary Device ID | 00817770021032 |
NIH Device Record Key | f88a30a8-8e98-4562-b9ef-ab87ee1b9fea |
Commercial Distribution Discontinuation | 2019-05-06 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Max-12 Oxygen Sensor |
Version Model Number | R109P45-012 |
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 | true |
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 | 00817770021032 [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 | 2 |
Public Version Date | 2019-05-07 |
Device Publish Date | 2019-01-14 |
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