STR CVR-4X26X76-4T-CFT/STD FM-CAL117-PU 23180

GUDID 00840828163101

STR CVR-4X26X76-4T-CFT/STD FM-CAL117-PU

CURBELL MEDICAL PRODUCTS, INC.

Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress Stretcher mattress

• Primary Device ID: 00840828163101
• NIH Device Record Key: e341f6c2-950e-410e-81ff-7d96ff32e46f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STR CVR-4X26X76-4T-CFT/STD FM-CAL117-PU
• Version Model Number: SMC-42676-4T-UF117-PU
• Catalog Number: 23180
• 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: false
• 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: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840828163101 [Primary]

FDA Product Code

• FPP: Stretcher, Hand-Carried

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: 2020-03-27
• Device Publish Date: 2020-03-19

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