PowerFlexx® Incubator Transporter

GUDID 00190790001209

PowerFlexx® Incubator Transporter, Red w/o Dropframe

FERNO-WASHINGTON, INC.

Ambulance stretcher, manual

• Primary Device ID: 00190790001209
• NIH Device Record Key: aea7a6ae-b393-4e30-8e53-cedfd7fc6925
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PowerFlexx® Incubator Transporter
• Version Model Number: 0163278
• 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: 937-382-1685
• Email: tscoordinator@ferno.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190790001209 [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 [PowerFlexx® Incubator Transporter]

• 00190790001216: PowerFlexx® Incubator Transporter, Blue w/o Dropframe
• 00190790001209: PowerFlexx® Incubator Transporter, Red w/o Dropframe
• 00190790001155: PowerFlexx® Incubator Transporter, Blue
• 00190790001148: PowerFlexx® Incubator Transporter, Red