Imprint™ 4 Penta™ Super Quick Heavy 71495

GUDID J001702011415070

3M™ ESPE™ Imprint™ 4 Penta™ Super Quick Heavy Intro Kit, 71495

3M Deutschland GmbH

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• Primary Device ID: J001702011415070
• NIH Device Record Key: 4df0dfb0-81b2-471c-b72f-18258106fb29
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Imprint™ 4 Penta™ Super Quick Heavy
• Version Model Number: 71495
• Catalog Number: 71495
• Company DUNS: 315731711
• Company Name: 3M Deutschland GmbH
• 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: false
• Expiration Date: true
• 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)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com
• Phone: +1(800)634-2249
• Email: 3Mhealthcarecompliance@mmm.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	J001702011415070 [Primary]

FDA Product Code

• EFD: AMALGAMATOR, DENTAL, AC-POWERED

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 7
• Public Version Date: 2020-09-22
• Device Publish Date: 2016-09-24

On-Brand Devices [Imprint™ 4 Penta™ Super Quick Heavy]

• J001702011415070: 3M™ ESPE™ Imprint™ 4 Penta™ Super Quick Heavy Intro Kit, 71495
• 04035077007801: 3M™ ESPE™ Imprint™ 4 Penta™ Super Quick Heavy Intro Kit, 71495