← Back to catalogue

Neodent

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 103.585Model Instrument

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

Identity

Trade Name
Neodent FDA UDI
Generic Name
Dental soft-tissue coring punch, reusable FDA UDI
Device Name
Drilling Instruments EUDAMED
NGM GUIDED SURGERY MUCOSA PUNCH FDA UDI
Model / Reference
103.585 EUDAMEDFDA UDI
Instrument EUDAMED
Description
NGM GUIDED SURGERY MUCOSA PUNCH FDA UDI

Identifiers

Catalog Number
103.585 FDA UDI
Primary DI / UDI-DI
07899878055624 EUDAMEDFDA UDI
Basic UDI-DI
987800084VX EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
Q0199 ODONTOLOGY DEVICES - OTHER EUDAMED
GMDN Term
Dental soft-tissue coring punch, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.3980 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

Category: Dental soft-tissue coring punch, reusable

Neodent 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 soft-tissue coring punch, 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 9142f5a8-73a2-42a6-901e-ed9fa6c1f221 36 fields · synced Jul 13, 2026
  • EUDAMED 9a79ff52-546f-4052-ac03-4feb9d5e45c6 61 fields · synced Jul 13, 2026