Identity

Trade Name
Nuvo FDA UDI
Generic Name
Surgical drill guide, single-use FDA UDI
Device Name
TREPHINE BUR GUIDE IF SP FDA UDI
Model / Reference
CD3002004 FDA UDI
Description
TREPHINE BUR GUIDE IF SP FDA UDI

Identifiers

Catalog Number
CD3002004 FDA UDI
Primary DI / UDI-DI
07899878058465 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Surgical drill guide, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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 — 5.0 Millimeter FDA UDI

Category: Surgical drill guide, single-use

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

Similar devices

Also classified as Surgical drill guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 3e3ee57a-4131-4820-950b-ed5a897aeb0d 36 fields · synced May 31, 2026