Universal Base 38213

GUDID 07332747096521

Universal Base CC NP 1.5mm

Nobel Biocare AB

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 07332747096521
• NIH Device Record Key: c5c20187-85cc-4901-844e-20b70c09ff81
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Universal Base
• Version Model Number: 38213
• Catalog Number: 38213
• Company DUNS: 353939929
• Company Name: Nobel Biocare AB
• Device Count: 1
• DM Exempt: true
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com
• Phone: +1(800)322-5001
• Email: us.customerservice@nobelbiocare.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07332747096521 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133731

FDA Product Code

• NHA: ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

Sterilization

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

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

[07332747096521]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-11-08
• Device Publish Date: 2015-09-17

On-Brand Devices [Universal Base]

• 07332747096576: Universal Base CC WP 3mm
• 07332747096569: Universal Base CC RP 3mm
• 07332747096552: Universal Base CC NP 3mm
• 07332747096545: Universal Base CC WP 1.5mm
• 07332747096538: Universal Base CC RP 1.5mm
• 07332747096521: Universal Base CC NP 1.5mm