JUMPER,36",P106 TO RJ45 (P808) 28879

GUDID 00840828190756

JUMPER,36",P106 TO RJ45 (P808)

CURBELL MEDICAL PRODUCTS, INC.

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• Primary Device ID: 00840828190756
• NIH Device Record Key: e336dbb1-eac6-48e5-b8ff-f07ad27c9272
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JUMPER,36",P106 TO RJ45 (P808)
• Version Model Number: JU36-178
• Catalog Number: 28879
• 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
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840828190756 [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: 2024-04-05
• Device Publish Date: 2024-03-28

Devices Manufactured by CURBELL MEDICAL PRODUCTS, INC.

• 00840828182294 - REUS,NCLR OXSMRT SPO2 SNSR,9.5',LG CLAM: 2024-04-18 REUS,NCLR OXSMRT SPO2 SNSR,9.5',LG CLAM
• 00840828182300 - REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG CLAM: 2024-04-18 REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG CLAM
• 00840828182317 - REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG SOFT: 2024-04-18 REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG SOFT
• 00840828182324 - REUS,NLCR OXSMRT SPO2 SNSR,3.3',SM SOFT: 2024-04-18 REUS,NLCR OXSMRT SPO2 SNSR,3.3',SM SOFT
• 00840828182331 - REUS,NLCR OXMAX SPO2 SNSR,9.5',LG CLAM: 2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,9.5',LG CLAM
• 00840828182348 - REUS,NLCR OXMAX SPO2 SNSR,3.3',LG CLAM: 2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,3.3',LG CLAM
• 00840828182355 - REUS,NLCR OXMAX SPO2 SNSR,9.5',LG SOFT: 2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,9.5',LG SOFT
• 00840828182362 - REUS,NLCR OXMAX SPO2 SNSR,3.3',LG SOFT: 2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,3.3',LG SOFT