30049

GUDID 07332747016352

Imm Prov Implant Disposable Twist Drill

Nobel Biocare AB

Fluted surgical drill bit, single-use, sterile

• Primary Device ID: 07332747016352
• NIH Device Record Key: bb7a961a-cd5c-47d6-a19e-4af825f3c79a
• Commercial Distribution Discontinuation: 2018-06-12
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 30049
• Catalog Number: 30049
• 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: 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)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	07332747016352 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K990846

FDA Product Code

• DZI: DRILL, BONE, POWERED

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-05-31
• Device Publish Date: 2016-09-17

Devices Manufactured by Nobel Biocare AB

• 07332747202991 - NobelProcera®: 2024-12-27 NobelProcera® Esthetic Zirconia Implant Bridge 2unit A1
• 07332747203004 - NobelProcera®: 2024-12-27 NobelProcera® Esthetic Zirconia Implant Bridge 3unit A1
• 07332747203011 - NobelProcera®: 2024-12-27 NobelProcera® Esthetic Zirconia Implant Bridge 4unit A1
• 07332747203028 - NobelProcera®: 2024-12-27 NobelProcera® Esthetic Zirconia Implant Bridge 5unit A1
• 07332747203035 - NobelProcera®: 2024-12-27 NobelProcera® Esthetic Zirconia Implant Bridge 6unit A1
• 07332747203042 - NobelProcera®: 2024-12-27 NobelProcera® Esthetic Zirconia Implant Bridge 7unit A1
• 07332747203059 - NobelProcera®: 2024-12-27 NobelProcera® Esthetic Zirconia Implant Bridge 8unit A1
• 07332747203066 - NobelProcera®: 2024-12-27 NobelProcera® Esthetic Zirconia Implant Bridge 9unit A1