← Back to catalogue

Nuvo

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref CD3003009Model Instrument

by JJGC Indústria e Comércio de Materiais Dentários S/A.

Identity

Trade Name
Nuvo FDA UDI
Generic Name
Dental implant reamer FDA UDI
Device Name
Drilling Instruments EUDAMED
BONE REMOVAL DRILL + ABUTMENT REMOVAL GUIDE CF NP FDA UDI
Model / Reference
CD3003009 EUDAMEDFDA UDI
Instrument EUDAMED
Description
BONE REMOVAL DRILL + ABUTMENT REMOVAL GUIDE CF NP FDA UDI

Identifiers

Catalog Number
CD3003009 FDA UDI
Primary DI / UDI-DI
07899878058533 EUDAMEDFDA UDI
Basic UDI-DI
987800093VY EUDAMED
FDA Product Code
DZA FDA UDI
EMDN Code
Z129099 VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - OTHER EUDAMED
GMDN Term
Dental implant reamer FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.4130 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 3.75 Millimeter FDA UDI

Category: Dental implant reamer

Nuvo by JJGC Indústria e Comércio de Materiais Dentários S/A. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant reamer.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI 0e71afdc-efdf-4220-be49-eba45e9877e3 37 fields · synced Sep 18, 2026
  • EUDAMED 4f9996af-e74f-462d-a252-8cf2edbc98a2 61 fields · synced Sep 18, 2026