LC Accu-Bar; STRIP, TEMPERATURE, FOREHEAD, LIQUI 989805623001

GUDID 20884838075089

Philips Medical Systems

Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use Liquid-crystal patient thermometer, single-use

• Primary Device ID: 20884838075089
• NIH Device Record Key: 3cd35abf-8da9-4d75-b948-4a809d114b63
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LC Accu-Bar; STRIP, TEMPERATURE, FOREHEAD, LIQUI
• Version Model Number: 989805623001
• Catalog Number: 989805623001
• Company DUNS: 078628040
• Company Name: Philips Medical Systems
• 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: 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(999)999-9999
• Email: xx@xx.xx
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• Phone: +1(999)999-9999
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	20884838075089 [Primary]

FDA Product Code

• KPD: STRIP, TEMPERATURE, FOREHEAD, LIQUID CRYSTAL

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: 2020-02-24
• Device Publish Date: 2016-09-21

Devices Manufactured by Philips Medical Systems

• 10884838000671 - Paper: 2021-11-18
• 00884838107199 - PageWriter: 2021-10-15
• 20884838013517 - NA: 2021-10-01
• 20884838013524 - NA: 2021-10-01
• 20884838091782 - Microstream Advance Adult Oral-Nasal CO2 Filter Line: 2021-08-02
• 20884838091829 - Microstream Advance Adult-Intermediate Bite Block CO2 Filter Line: 2021-08-02
• 20884838091836 - Microstream Advance Adult-Pediatric Intubated CO2 Filter Line: 2021-08-02
• 20884838091850 - Microstream Advance Adult-Pediatric Intubated CO2 Filter Line: 2021-08-02