35X ProFlexx®

GUDID 00190790000325

Ambulance stretcher, manual

Primary Device ID	00190790000325
NIH Device Record Key	ee09b12c-f313-4423-96d3-4690b989efcd
Commercial Distribution Status	In Commercial Distribution
Brand Name	35X ProFlexx®
Version Model Number	0015703
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

Device Issuing Agency	Device ID
GS1	00190790000325 [Primary]

FPO	Stretcher, Wheeled

Steralize Prior To Use	false
Device Is Sterile	false

00190790000332	35X ProFlexx®, EFNY
00190790000325	35X ProFlexx®, Blue w/Univ Side Arm
00190790000318	35X ProFlexx®, Red w/Univ Side Arm
00190790000301	35X ProFlexx®, Blue
00190790000295	35X ProFlexx®, Red