35X-NM ProFlexx®

GUDID 00190790000349

35X-NM ProFlexx®, Non Magnetic

FERNO-WASHINGTON, INC.

Ambulance stretcher, manual

• Primary Device ID: 00190790000349
• NIH Device Record Key: 1aa7b574-5311-4cd0-840c-4fab65e641a6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 35X-NM ProFlexx®
• Version Model Number: 0015788
• Company DUNS: 004239034
• Company Name: FERNO-WASHINGTON, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• 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
• Email: complaintcoordinator@ferno.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190790000349 [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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-22

On-Brand Devices [35X-NM ProFlexx®]

• 00190790000356: 35X-NM ProFlexx®, Non Magnetic
• 00190790000349: 35X-NM ProFlexx®, Non Magnetic