SPO2 AD CB,SPACELABS 10M,DB9F,3M 29124

GUDID 00840828192514

SPO2 AD CB,SPACELABS 10M,DB9F,3M

CURBELL MEDICAL PRODUCTS, INC.

Electrical-only medical device connection cable, reusable

• Primary Device ID: 00840828192514
• NIH Device Record Key: c276a14a-97eb-4f46-a1c7-c9e9b59a9f5d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SPO2 AD CB,SPACELABS 10M,DB9F,3M
• Version Model Number: OCT017-L
• Catalog Number: 29124
• Company DUNS: 796452311
• Company Name: CURBELL MEDICAL PRODUCTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• 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
• 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	00840828192514 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222370

FDA Product Code

• DSA: Cable, Transducer And Electrode, Patient, (Including Connector)

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: 2024-07-29
• Device Publish Date: 2024-07-19

Devices Manufactured by CURBELL MEDICAL PRODUCTS, INC.

• 00840828193221 - GEN4 DIGITAL: 2024-11-18 GEN4 DIGITAL
• 00840828193238 - GEN4 INTERACTIVE: 2024-11-18
• 00840828193245 - CLICK,8 PIN DIN,8 FT,WHITE,TT WIRING: 2024-11-18
• 00840828193252 - CLICK,8 PIN DIN,20 FT,WHITE,TT WIRING: 2024-11-18
• 00840828193269 - RESPONDER 5, INTERACTIVE: 2024-11-18
• 00840828193276 - CLICK,1/4" PLUG (P102),6 IN,WHITE: 2024-11-18
• 00840828193283 - CLICK,1/4" PLUG (P102),20 FT,WHITE: 2024-11-18
• 00840828193290 - CLICK,8 PIN DIN,6 IN,WHITE,TT WIRING: 2024-11-18