35X-IT ProFlexx® Incubator Transporter

GUDID 00190790001193

35X-IT ProFlexx® Incubator Transporter, Blue w/o Dropframe

FERNO-WASHINGTON, INC.

Ambulance stretcher, manual

• Primary Device ID: 00190790001193
• NIH Device Record Key: 7aaf4459-3af0-4bf8-ac52-da0342cb6998
• Commercial Distribution Discontinuation: 2017-06-15
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: 35X-IT ProFlexx® Incubator Transporter
• Version Model Number: 0163276
• 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
• Email: complaintcoordinator@ferno.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190790001193 [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 [35X-IT ProFlexx® Incubator Transporter]

• 00190790001193: 35X-IT ProFlexx® Incubator Transporter, Blue w/o Dropframe
• 00190790001186: 35X-IT ProFlexx® Incubator Transporter, Red w/o Dropframe
• 00190790001179: 35X-IT ProFlexx® Incubator Transporter, Blue w/Dropframe
• 00190790001162: 35X-IT ProFlexx® Incubator Transporter, Red w/Dropframe