Primary Device ID | 00190790002183 |
NIH Device Record Key | b2fd564e-1415-45dd-af4d-f0c433e972b7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | POWER X1 |
Version Model Number | 0015807 |
Company DUNS | 004239034 |
Company Name | FERNO-WASHINGTON, 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 |
Phone | 937-382-1685 |
tscoordinator@ferno.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00190790002183 [Primary] |
FPO | Stretcher, Wheeled |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-10 |
Device Publish Date | 2018-08-10 |
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00190790002183 - POWER X1 | 2018-09-10POWER X1 |
00190790002183 - POWER X1 | 2018-09-10 POWER X1 |