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Neodent

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 108.237Model Instrument

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

Identity

Trade Name
Neodent FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, reusable FDA UDI
Device Name
Reusable Implant Impression Copings EUDAMED
SCAN BASE C ZI 4.5 mm FDA UDI
Model / Reference
Instrument EUDAMED
108.237 EUDAMED
108.337 FDA UDI
Description
SCAN BASE C ZI 4.5 mm FDA UDI

Identifiers

Catalog Number
108.337 FDA UDI
Primary DI / UDI-DI
07899878061137 EUDAMEDFDA UDI
Basic UDI-DI
987800095W4 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
Q0199 ODONTOLOGY DEVICES - OTHER EUDAMED
GMDN Term
Dental implant suprastructure, temporary, preformed, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 4.5 Millimeter FDA UDI

Category: Dental implant suprastructure, temporary, preformed, 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 implant suprastructure, temporary, preformed, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 572ec303-52b3-421d-93f4-fc460e46632f 37 fields · synced Jul 20, 2026
  • EUDAMED a1f9e609-0891-4f20-85b4-fd1f90c744d7 61 fields · synced Jul 20, 2026