Primary Device ID | 10862229000202 |
NIH Device Record Key | c7e62a9d-facb-423a-819a-33185aa03e7c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Posey Cufflators Endotracheal Tube Inflator and Manometer |
Version Model Number | 8199 |
Company DUNS | 008503294 |
Company Name | POSEY PRODUCTS, 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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10862229000202 [Primary] |
BSK | Cuff, Tracheal Tube, Inflatable |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2022-10-20 |
Device Publish Date | 2015-10-31 |
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