Primary Device ID | 00817770025627 |
NIH Device Record Key | eb3b73da-2e88-420b-9c21-601bdfb060e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BlenderBuddy |
Version Model Number | BlenderBuddy |
Catalog Number | R219P20-006 |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817770025627 [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 | 2021-11-02 |
Device Publish Date | 2021-10-25 |
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