Primary Device ID | 00817770025757 |
NIH Device Record Key | b8181007-7c55-4ec1-aaeb-060fabe1196e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Flowmeter Manifold |
Version Model Number | IV Pole |
Catalog Number | R220P10-009 |
Company DUNS | 169911828 |
Company Name | MAXTEC, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
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 | 00817770025757 [Primary] |
CAX | Flowmeter, Tube, Thorpe, Back-Pressure Compensated |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-16 |
Device Publish Date | 2023-06-08 |
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