Procera® 10-4022

GUDID 07332747100488

Procera Abutment Ti hex 4.3

Nobel Biocare AB

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 07332747100488
• NIH Device Record Key: 1afb7282-da85-460b-be34-ec558c1fd176
• Commercial Distribution Discontinuation: 2016-06-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Procera®
• Version Model Number: 10-4022
• Catalog Number: 10-4022
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07332747100488 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K974150

FDA Product Code

• NHA: ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

Sterilization

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

[07332747100488]

Moist Heat or Steam Sterilization

[07332747100488]

Moist Heat or Steam Sterilization

[07332747100488]

Moist Heat or Steam Sterilization

[07332747100488]

Moist Heat or Steam Sterilization

[07332747100488]

Moist Heat or Steam Sterilization

[07332747100488]

Moist Heat or Steam Sterilization

[07332747100488]

Moist Heat or Steam Sterilization

[07332747100488]

Moist Heat or Steam Sterilization

[07332747100488]

Moist Heat or Steam Sterilization

[07332747100488]

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 [Procera®]

• 07332747119770: Procera® Imp Br Zr Imp Lev 5 unit Int
• 07332747119763: Procera® Imp Br Zr Imp Lev 6 unit Int
• 07332747119756: Procera® Imp Br Zr Imp Lev 7unit Intense
• 07332747119749: Procera Implant Bridge Zr Imp Lev 8 unit
• 07332747119732: Procera® Imp Br Zr Imp Lev 8 unit Med
• 07332747119725: Procera® Imp Br Zr Imp Lev 8 unit Int
• 07332747119718: Procera® Imp Br Zr Imp Lev 9 unit Med
• 07332747119701: Procera® Imp Br Zr Imp Lev 9 unit Int
• 07332747119695: Procera® Imp Br Zr Imp Lev 10 unit Int
• 07332747119688: Procera® Imp Br Zr Imp Lev 11 unit Med
• 07332747119671: Procera® Imp Br Zr Imp Lev 11 unit Int
• 07332747119664: Procera® Imp Br Zr Imp Lev 12 unit Int
• 07332747119657: Procera® Imp Br Zr Imp Lev 13 unit Med
• 07332747119640: Procera® Imp Br Zr Imp Lev 13 unit Int
• 07332747119633: Procera® Imp Br Zr Imp Lev 14 unit Int
• 07332747119343: Procera Bridge Zirconia 9 unit
• 07332747119336: Procera® Bridge Zirconia 9 unit Medium
• 07332747119329: Procera® Bridge Zirconia 9 unit Intense
• 07332747119312: Procera® Bridge Zirconia 9 unit Light
• 07332747119305: Procera Bridge Zirconia 10 unit
• 07332747119299: Procera® Bridge Zirconia 10 unit Medium
• 07332747119282: Procera® Bridge Zirconia 10 unit Intense
• 07332747119275: Procera® Bridge Zirconia 10 unit Light
• 07332747119268: Procera Bridge Zirconia 11 unit
• 07332747119251: Procera® Bridge Zirconia 11 unit Medium
• 07332747119244: Procera® Bridge Zirconia 11 unit Intense
• 07332747119237: Procera® Bridge Zirconia 11 unit Light
• 07332747119220: Procera Bridge Zirconia 12 unit
• 07332747119213: Procera® Bridge Zirconia 12 unit Medium
• 07332747119206: Procera® Bridge Zirconia 12 unit Intense
• 07332747119190: Procera® Bridge Zirconia 12 unit Light
• 07332747119183: Procera Bridge Zirconia 13 unit
• 07332747119176: Procera® Bridge Zirconia 13 unit Medium
• 07332747119169: Procera® Bridge Zirconia 13 unit Intense
• 07332747119152: Procera® Bridge Zirconia 13 unit Light
• 07332747119145: Procera Bridge Zirconia 14 unit
• 07332747119138: Procera® Bridge Zirconia 14 unit Medium
• 07332747119121: Procera® Bridge Zirconia 14 unit Intense
• 07332747119114: Procera® Bridge Zirconia 14 unit Light
• 07332747102307: Procera® Abutment Zr NobelActive Int NP
• 07332747102291: Procera® Ab Zr NobelActive Int NP Wax-up
• 07332747102284: Procera® Abutment Zr NobelActive Int RP
• 07332747102277: Procera® Ab Zr NobelActive Int RP Wax-up
• 07332747102260: Procera® Abutment Ti NobelActive Int NP
• 07332747102253: Procera® Ab Ti NobelActive Int NP Wax-up
• 07332747102246: Procera® Abutment Ti NobelActive Int RP
• 07332747102239: Procera® Ab Ti NobelActive Int RP Wax-up
• 07332747100594: PROCERA ABUTMENT TI BR NEMARK SYSTEM RP
• 07332747100587: PROCERA ABUTMENT TI BR NEMARK SYSTEM NP
• 07332747100570: PROCERA ABUTMENT TI BR NEMARK SYSTEM WP