BluPRO® TL-271T3

GUDID 10841983102711

SpO2 probe Adults (30 kg or more) Finger or toe, disposable, 160cm cable

NIHON KOHDEN AMERICA, INC.

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• Primary Device ID: 10841983102711
• NIH Device Record Key: 5f477f42-3b8a-4635-ac98-74642ddf6720
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BluPRO®
• Version Model Number: TL-271T3
• Catalog Number: TL-271T3
• Company DUNS: 021063219
• Company Name: NIHON KOHDEN AMERICA, INC.
• Device Count: 24
• 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: true
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com
• Phone: +1(800)325-0283
• Email: info@nkusa.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841983102714 [Unit of Use]
GS1	10841983102711 [Primary]

FDA Product Code

• GWQ: Full-montage Standard Electroencephalograph

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-11-10
• Device Publish Date: 2016-09-19

On-Brand Devices [BluPRO®]

• 00841983102752: Finger probe Adult, child (20 kg or more) Finger or toe
• 00841983102691: Multi-site probe Adults, child (3 kg or more)
• 00841983102684: Finger probe Adult, child (20kg or more) Finger
• 04931921019696: Multi-site probe Adults, child (3 kg or more)
• 10841983102742: SpO2 probe Child / Infant (from 3 to 20 kg) Finger or toe, disposable
• 10841983102735: SpO2 probe Adults (40 kg or more) Finger or toe, disposable
• 10841983102728: SpO2 probe Child (from 10 to 50 kg) Finger or toe, disposable
• 10841983102711: SpO2 probe Adults (30 kg or more) Finger or toe, disposable, 160cm cable
• 10841983102704: SpO2 probe Adults (30 kg or more) Finger or toe, disposable, 80cm cable