Straumann® TL WN-compatible 9001303

GUDID 00842092181904

Straumann® TL WN-compatible Digital Analog Kit contains: 1 Straumann® TL WN-compatible Digital Analog 1 Digital Analog Base Screw

Preat Corporation

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• Primary Device ID: 00842092181904
• NIH Device Record Key: ee63fc7a-0d65-47a3-a316-637c10caf78c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Straumann® TL WN-compatible
• Version Model Number: 9001303
• Catalog Number: 9001303
• Company DUNS: 117776048
• Company Name: Preat Corporation
• 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: true
• Device Combination Product: false
• Single Use: true
• 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) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com
• Phone: +1 (800) 232-7732
• Email: info@preat.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00842092181898 [Primary]
GS1	00842092181904 [Package]; Contains: 00842092181898; Package: Pack [10 Units]; In Commercial Distribution

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

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: 2024-02-14
• Device Publish Date: 2024-02-06

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