Littmann® Telesteth™ TS1200CL

GUDID 00707387766597

TS1200CL TELESTETH SOFTWARE HOSTED LICENSE

3M COMPANY

Stethoscope application software

• Primary Device ID: 00707387766597
• NIH Device Record Key: e185c37a-0bf0-4ae4-9155-6080807a391e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Littmann® Telesteth™
• Version Model Number: TS1200CL
• Catalog Number: TS1200CL
• Company DUNS: 830016148
• Company Name: 3M COMPANY
• 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)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00707387766597 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K120704

FDA Product Code

• DRG: TRANSMITTERS AND RECEIVERS, PHYSIOLOGICAL SIGNAL, RADIOFREQUENCY

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: 2018-07-06
• Device Publish Date: 2016-09-24

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