SPO2 AD CB,SPCELBS 10M OXMX,DB9F OXMX,3M 29125

GUDID 00840828192521

SPO2 AD CB,SPCELBS 10M OXMX,DB9F OXMX,3M

CURBELL MEDICAL PRODUCTS, INC.

Electrical-only medical device connection cable, reusable

• Primary Device ID: 00840828192521
• NIH Device Record Key: e95a40bf-80f4-4cb5-813b-1cb8e9871b41
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SPO2 AD CB,SPCELBS 10M OXMX,DB9F OXMX,3M
• Version Model Number: OCT017-OL
• Catalog Number: 29125
• 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	00840828192521 [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.

• 00840828180276 - 3701 P37,4FT,1TO1,90 DEG BED END,STKR: 2026-02-02 3701 P37,4FT,1TO1,90 DEG BED END,STKR
• 00840828180283 - 102 P37,2FT,NURSE ONLY,STKR: 2026-02-02 102 P37,2FT,NURSE ONLY,STKR
• 00840828180290 - 02 P37,6FT,NURSE ONLY,STKR: 2026-02-02 02 P37,6FT,NURSE ONLY,STKR
• 00840828180306 - 3701 P37,2FT,1TO1,90 DEG BED END,STKR: 2026-02-02 3701 P37,2FT,1TO1,90 DEG BED END,STKR
• 00840828180313 - 3701 P37,6FT,1TO1,90 DEG BED END,STKR: 2026-02-02 3701 P37,6FT,1TO1,90 DEG BED END,STKR
• 00840828180320 - 103 P37,2FT,NURSE ONLY,INLINE,STKR: 2026-02-02 103 P37,2FT,NURSE ONLY,INLINE,STKR
• 00840828180337 - 103 P37,6FT,NURSE ONLY,INLINE,STKR: 2026-02-02 103 P37,6FT,NURSE ONLY,INLINE,STKR
• 00840828180344 - 800 P37,R4,2L,22 OHM,2FT,STKR: 2026-02-02 800 P37,R4,2L,22 OHM,2FT,STKR