Primary Device ID | 05059441900665 |
NIH Device Record Key | ca8eee42-c88d-41e3-ba63-2d260c04b70b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Evenda |
Version Model Number | EN21AFD0ASQAACA |
Company DUNS | 355804758 |
Company Name | Arjohuntleigh AB |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05059441900665 [Primary] |
FNL | BED, AC-POWERED ADJUSTABLE HOSPITAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-19 |
Device Publish Date | 2023-06-10 |
05059441900665 | Medical Bed - Evenda -Long Term Care |
05059441307174 | Medical Bed - Evenda -Long Term Care -Narrow |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EVENDA 79298289 not registered Live/Pending |
Arjo IP Holding AB 2020-10-02 |