Primary Device ID | 00850020142446 |
NIH Device Record Key | 02a02bec-422b-45d0-8b5e-d3e6f50c86e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AE Elevating Treatment Table |
Version Model Number | A4201-EL |
Company DUNS | 826316098 |
Company Name | PIVOTAL HEALTH SOLUTIONS, INC. |
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 | 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 | 00850020142446 [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 | 2025-08-20 |
Device Publish Date | 2025-08-12 |
00850020142446 - AE Elevating Treatment Table | 2025-08-20 |
00850020142446 - AE Elevating Treatment Table | 2025-08-20 |
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