Nuvo CD1002002

GUDID 07899878045632

PRE-MOUNTED IF SURGICAL KIT

JJGC Indústria e Comércio de Materiais Dentários S/A.

Dental/maxillofacial surgical procedure kit, non-medicated, reusable

• Primary Device ID: 07899878045632
• NIH Device Record Key: f6b67ba1-0101-4067-8aca-cde26011800c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nuvo
• Version Model Number: CD1002002
• Catalog Number: CD1002002
• Company DUNS: 906713888
• Company Name: JJGC Indústria e Comércio de Materiais Dentários S/A.
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com
• Phone: +1(855)412-8883
• Email: customerservice.us@instradent.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07899878045632 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192670

FDA Product Code

• KCT: Sterilization wrap containers, trays, cassettes & other accessories

Sterilization

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

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

[07899878045632]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-18
• Device Publish Date: 2023-08-10

On-Brand Devices [Nuvo]

• 07899878042860: PROSTHETIC CASSETTE
• 07899878042143: PROSTHETIC SCREW MULTI UNIT PROSTHESIS
• 07899878041443: DISTAL BAR MULTI UNIT SCREW RETAINED ABUT. 4.8
• 07899878041405: ONE STEP HYBRID COPING(CAST) MULTI UNIT SCREW RETAINED ABUT.
• 07899878041399: ONE STEP HYBRID COPING(Ti) MULTI UNIT SCREW RETAINED ABUT.
• 07899878041382: ONE STEP HYBRID COPING(CUZN) MULTI UNIT SCREW RETAINED ABUT.
• 07899878041368: TITANIUM COPING MULTI UNIT SCREW RETAINED ABUT.
• 07899878041344: COCR COPING MULTI UNIT SCREW RETAINED ABUT.
• 07899878039761: TITANIUM BASE FOR BRIDGE IF
• 07899878039754: TITANIUM BASE FOR BRIDGE IF
• 07899878039747: TITANIUM BASE FOR BRIDGE IF
• 07899878039730: TITANIUM BASE IF
• 07899878039723: TITANIUM BASE IF
• 07899878039716: TITANIUM BASE IF
• 07899878039419: PRE MILLED ABUTMENT TITAN. BLANK/MEDENTIKA HOLDER IF
• 07899878039402: PRE MILLED ABUTMENT TITAN. BLANK/MEDENTIKA HOLDER IF
• 07899878039396: PRE MILLED ABUTMENT TITAN. BLANK/MEDENTIKA HOLDER IF
• 07899878039389: PRE MILLED ABUTMENT TITAN. BLANK/MEDENTIKA HOLDER IF
• 07899878039129: TITANIUM BASE FOR BRIDGE IF
• 07899878039112: TITANIUM BASE FOR BRIDGE IF
• 07899878039105: TITANIUM BASE FOR BRIDGE IF
• 07899878039099: TITANIUM BASE IF
• 07899878039075: TITANIUM BASE IF
• 07899878039068: TITANIUM BASE FOR BRIDGE IF
• 07899878039051: TITANIUM BASE FOR BRIDGE IF
• 07899878044246: PROTECTION CYLINDER FOR MULTI UNIT SCREW RETAINED ABUT.
• 07899878040989: ATTACHMENT REMOVABLE PROSTHESIS IF
• 07899878040972: ATTACHMENT REMOVABLE PROSTHESIS IF
• 07899878040965: ATTACHMENT REMOVABLE PROSTHESIS IF
• 07899878040958: ATTACHMENT REMOVABLE PROSTHESIS IF
• 07899878040743: MULTI UNIT SCREW RETAINED ABUTMENT SCREW IF
• 07899878040736: MULTI UNIT SCREW RETAINED ABUTMENT SCREW IF
• 07899878040729: PROSTHETIC SCREW IF
• 07899878040712: PROSTHETIC SCREW IF
• 07899878040705: ATTACHMENT REMOVABLE PROSTHESIS IF
• 07899878040699: ATTACHMENT REMOVABLE PROSTHESIS IF
• 07899878040682: ATTACHMENT REMOVABLE PROSTHESIS IF
• 07899878040675: ATTACHMENT REMOVABLE PROSTHESIS IF
• 07899878040668: ATTACHMENT REMOVABLE PROSTHESIS IF
• 07899878040651: ATTACHMENT REMOVABLE PROSTHESIS IF
• 07899878040484: UCLA ABUTMENT COCR FOR BRIDGE IF(5UN)
• 07899878040477: UCLA ABUTMENT COCR FOR CROWN IF(5UN)
• 07899878040460: UCLA ABUTMENT COCR FOR BRIDGE IF(5UN)
• 07899878040453: UCLA ABUTMENT COCR FOR CROWN IF(5UN)
• 07899878040446: UCLA ABUTMENT COCR FOR BRIDGE IF(5UN)
• 07899878040439: UCLA ABUTMENT COCR FOR CROWN IF(5UN)
• 07899878039822: TITANIUM TEMPORARY ABUTMENT FOR BRIDGE IF
• 07899878039815: TITANIUM TEMPORARY ABUTMENT FOR CROWN IF
• 07899878039808: TITANIUM TEMPORARY ABUTMENT FOR BRIDGE IF
• 07899878039792: TITANIUM TEMPORARY ABUTMENT FOR CROWN IF