FDA UDI Not in Commercial Distribution 🇺🇸 United States

PowerFlexx®

DI: 00190790000172 · Model: 0015651 · FERNO-WASHINGTON, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PowerFlexx®
Primary DI
00190790000172
Version / Model
0015651
Company Name
FERNO-WASHINGTON, INC.
Labeler DUNS
004239034
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-22
Public Version
4
Public Version Date
2022-08-30
Public Version Status
Update
Public Device Record Key
b897096d-f17a-4689-a1e4-5c0a9d902a7b
Distribution End Date
2019-11-26

Device Description

PowerFlexx® Powered Cot, Red

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FPO Stretcher, Wheeled

GMDN Terms

Code Name
60487 Ambulance stretcher, electrohydraulic

Identifiers

Type ID
Primary 00190790000172

Customer Contacts

Phone
937-382-1685
Phone
937-283-2950