DISP NK COMP SPO2 SNSR,TL-271T,ADLT,39",WHT FM,NON-STRL,EACH 28171

GUDID 10840828185988

DISP NK COMP SPO2 SNSR,TL-271T3,ADLT,63",CLR FLM,NON-STRL,EACH

CURBELL MEDICAL PRODUCTS, INC.

Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use Pulse oximeter probe, single-use

• Primary Device ID: 10840828185988
• NIH Device Record Key: 11c13adb-7044-44dc-bbe1-1fe15db58ec9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DISP NK COMP SPO2 SNSR,TL-271T,ADLT,39",WHT FM,NON-STRL,EACH
• Version Model Number: CSA027DA-P200
• Catalog Number: 28171
• Company DUNS: 796452311
• Company Name: CURBELL MEDICAL PRODUCTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com
• Phone: 1-800-235-7500
• Email: mwinter@curbellmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840828185981 [Primary]
GS1	10840828185988 [Package]; Contains: 00840828185981; Package: Case [30 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182220

FDA Product Code

• DQA: Oximeter
• 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: 2023-08-07
• Device Publish Date: 2023-07-28

On-Brand Devices [DISP NK COMP SPO2 SNSR,TL-271T,ADLT,39",WHT FM,NON-STRL,EACH]

• 10840828185988: DISP NK COMP SPO2 SNSR,TL-271T3,ADLT,63",CLR FLM,NON-STRL,EACH
• 10840828185971: DISP NK COMP SPO2 SNSR,TL-271T,ADLT,39",WHT FM,NON-STRL,EACH