800,102 P37,R4,BE,2L,STKR 22568

GUDID 00840828161992

800,102 P37,R4,BE,2L,STKR

CURBELL MEDICAL PRODUCTS, INC.

Electrical mains power extension cable

• Primary Device ID: 00840828161992
• NIH Device Record Key: 0645521f-0232-4db8-80a7-88590b506081
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 800,102 P37,R4,BE,2L,STKR
• Version Model Number: 3001-990-856
• Catalog Number: 22568
• 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	00840828161992 [Primary]

FDA Product Code

• ILQ: System, Communication, Powered

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-08-30
• Device Publish Date: 2018-07-30

On-Brand Devices [800,102 P37,R4,BE,2L,STKR]

• 00840828161992: 800,102 P37,R4,BE,2L,STKR
• 00840828157551: 800,102 P37,R4,BE,2L,STKR
• 00840828181334: 800,102 P37,R4,BE,2L,STKR
• 00840828181679: 800,102 P37,R4,BE,2L,STKR