PowerFlexx®
GUDID 00190790000202
PowerFlexx® Powered Cot, Blue w/Univ Side Arm
FERNO-WASHINGTON, INC.
Ambulance stretcher, electrohydraulic| Primary Device ID | 00190790000202 |
| NIH Device Record Key | 252ec2fa-bc9a-489c-9585-3c4da876a2c4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PowerFlexx® |
| Version Model Number | 0015729 |
| 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 |
Customer Support Contacts
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com | |
| Phone | 937-283-2950 |
| complaintcoordinator@ferno.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00190790000202 [Primary] |
FDA Product Code
| FPO | Stretcher, Wheeled |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-10 |
| Device Publish Date | 2016-08-22 |
On-Brand Devices [PowerFlexx®]
| 00190790000288 | PowerFlexx®, Powered Cot, Blue Intl CE |
| 00190790000271 | PowerFlexx® Powered Cot, Red Intl CE ICS |
| 00190790000264 | PowerFlexx® Powered Cot, Red Intl CE |
| 00190790000257 | PowerFlexx® Powered Cot, Blue ST w/Univ Side Arm |
| 00190790000240 | PowerFlexx® Powered Cot, Red ST w/Univ Side Arm |
| 00190790000233 | PowerFlexx® Powered Cot, Blue ST |
| 00190790000226 | PowerFlexx® Powered Cot, Red ST |
| 00190790000219 | PowerFlexx® Powered Cot, Platinum w/Univ Side Arm |
| 00190790000202 | PowerFlexx® Powered Cot, Blue w/Univ Side Arm |
| 00190790000196 | PowerFlexx® Powered Cot, Red w/Univ Side Arm |
| 00190790000189 | PowerFlexx® Powered Cot, Blue |
| 00190790000172 | PowerFlexx® Powered Cot, Red |
Trademark Results [PowerFlexx]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 POWERFLEXX 78493774 3088721 Live/Registered |
Ferno-Washington, Inc. 2004-10-04 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.