Littmann® Classic III™ 5620C

GUDID 00197998470486

Littmann® Classic III™ Stethoscope, 5620C, Stainless-finishChestpiece, Satin-finish Black Tube

Solventum US LLC

Mechanical external stethoscope

• Primary Device ID: 00197998470486
• NIH Device Record Key: ab912448-035d-454d-88b1-93380d14746d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Littmann® Classic III™
• Version Model Number: 5620C
• Catalog Number: 5620C
• Company DUNS: 119004140
• Company Name: Solventum US LLC
• 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: 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com
• Phone: +1(800)634-2249
• Email: regulatoryrequests@solventum.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00197998470479 [Primary]
GS1	00197998470486 [Package]; Contains: 00197998470479; Package: [1 Units]; In Commercial Distribution

FDA Product Code

• LDE: STETHOSCOPE, MANUAL

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: 2026-02-11
• Device Publish Date: 2026-02-03

On-Brand Devices [Littmann® Classic III™]

• 00197998470523: Littmann® Classic III™ Stethoscope, 5623C, Stainless-finishChestpiece, Satin-finish Caribbean
• 00197998470509: Littmann® Classic III™ Stethoscope, 5648C, Stainless-finishChestpiece, Satin-finish Raspberry
• 00197998470486: Littmann® Classic III™ Stethoscope, 5620C, Stainless-finishChestpiece, Satin-finish Black Tub