419 P37,GE,2LD,STKR 179

GUDID 00840828100366

419 P37,GE,2LD,STKR

CURBELL MEDICAL PRODUCTS, INC.

Electrical mains power extension cable

• Primary Device ID: 00840828100366
• NIH Device Record Key: 0ee1762e-499c-461b-8727-13661be76efc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 419 P37,GE,2LD,STKR
• Version Model Number: 3001-990-404
• Catalog Number: 179
• Company DUNS: 796452311
• Company Name: CURBELL MEDICAL PRODUCTS, 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: true
• Serial Number: false
• 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: 1-800-235-7500
• Email: mwinter@curbell.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840828100366 [Primary]

FDA Product Code

• ILQ: System, Communication, Powered

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: 2016-09-24

On-Brand Devices [419 P37,GE,2LD,STKR]

• 00840828100366: 419 P37,GE,2LD,STKR
• 00840828181303: 419 P37,GE,2LD,STKR
• 00840828181648: 419 P37,GE,2LD,STKR