3M™ Littmann™ 8493

GUDID 50707387792430

3M™ Littmann™ Core Stethoscope, 8493, Black, EK

3M COMPANY

Electronic stethoscope

• Primary Device ID: 50707387792430
• NIH Device Record Key: 620dc003-0313-4677-a196-5787851f12e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3M™ Littmann™
• Version Model Number: 8493
• Catalog Number: 8493
• Company DUNS: 830016148
• Company Name: 3M COMPANY
• 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: 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)228-3957
• Email: 3Mhealthcarecompliance@mmm.com
• 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	00707387792435 [Primary]
GS1	50707387792430 [Package]; Contains: 00707387792435; Package: BOX [3 Units]; In Commercial Distribution

FDA Product Code

• DQD: STETHOSCOPE, ELECTRONIC

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-08-07
• Device Publish Date: 2022-12-08

Devices Manufactured by 3M COMPANY

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• 50605861085880 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550A2, A2, 0.2 g, Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS
• 50605861085897 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550A3, A3, 0.2 g, Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS
• 50605861085903 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550A3.5, A3.5, 0.2 g, Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS
• 50605861085910 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550A4, A4, 0.2 g Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS
• 50605861085927 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550B1, B1, 0.2 g Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS
• 50605861085934 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550B2, B2, 0.2 g Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS
• 50605861085941 - 3M™: 2025-09-17 3M™ Filtek™ Universal Restorative, 6550D3, D3, 0.2 g Capsule, 20/BT, 1 BT/BAG, 10 BAG/CS