Primary Device ID | 00853061006234 |
NIH Device Record Key | bf0b1ef3-c9fe-4e49-bd02-71e3fac465e3 |
Commercial Distribution Discontinuation | 2019-05-06 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | MicroMax |
Version Model Number | R203P14-004 |
Company DUNS | 169911828 |
Company Name | MAXTEC, 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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
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 |
Storage Environment Atmospheric Pressure | Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Storage Environment Atmospheric Pressure | Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00853061006234 [Primary] |
BZR | Mixer, Breathing Gases, Anesthesia Inhalation |
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 | 2015-11-18 |
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