← Back to catalogue

Nuvo

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref CD0330008Model Instrument

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

Identity

Trade Name
Nuvo FDA UDI
Generic Name
Surgical drill guide, reusable FDA UDI
Device Name
Surgically Invasive Accessories EUDAMED
DRILL STOP 3.5X11.5 mm FDA UDI
Model / Reference
CD0330008 EUDAMEDFDA UDI
Instrument EUDAMED
Description
DRILL STOP 3.5X11.5 mm FDA UDI

Identifiers

Catalog Number
CD0330008 FDA UDI
Primary DI / UDI-DI
07899878045458 EUDAMEDFDA UDI
Basic UDI-DI
987800054VN EUDAMED
FDA Product Code
DZA FDA UDI
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical drill guide, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA 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

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 11.5 Millimeter FDA UDI
Outer Diameter — 3.5 Millimeter FDA UDI

Category: Surgical drill guide, reusable

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 Surgical drill guide, reusable.

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 236f9523-ea66-465a-afa8-72af642078c5 37 fields · synced Jul 9, 2026
  • EUDAMED 88ca6a05-9bbb-4ca3-b5a2-f417d6883787 61 fields · synced Jul 9, 2026