Primary Device ID | 00817770024217 |
NIH Device Record Key | 0ce7ff95-c4ba-4078-bcf2-38f94231f7bb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Flowmeter Manifold |
Version Model Number | Acrylic 0-70 White |
Catalog Number | R220P01-201 |
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 | false |
Device Combination Product | false |
Single Use | false |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817770024217 [Primary] |
BXY | Flowmeter, Calibration, Gas |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-03-17 |
Device Publish Date | 2021-03-09 |
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