Primary Device ID | 00840314810953 |
NIH Device Record Key | 3b49dbd5-dcf9-4005-ad9a-2ea795871433 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Titan Premier 3-Section Treatment Table |
Version Model Number | 6084-BK |
Company DUNS | 001892660 |
Company Name | Hausmann Enterprises, 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 | false |
Serial Number | true |
Manufacturing Date | false |
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 | 00840314810953 [Primary] |
INQ | Table, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-14 |
Device Publish Date | 2023-12-06 |
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