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Neoss Implant System

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 51174

by Neoss, Ltd.

Identity

Trade Name
Neoss® Guide - Implant Mount SP, Ø6.0 S9 - 2 pcs EUDAMED
Neoss Implant System FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Manual Driver EUDAMED
Neoss® Guide – Implant Mount SP, Ø6.0 S9 – 2 pcs FDA UDI
Model / Reference
51174 EUDAMEDFDA UDI
Description
Neoss® Guide – Implant Mount SP, Ø6.0 S9 – 2 pcs FDA UDI

Identifiers

Catalog Number
51174 FDA UDI
Primary DI / UDI-DI
05060440332821 EUDAMEDFDA UDI
Basic UDI-DI
506044033N0045N7 EUDAMED
Direct Marketing DI
05060440332821 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Surgical screwdriver, 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical screwdriver, reusable

Neoss Implant System by Neoss, Ltd. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neoss, Ltd.

Sources (2)

  • FDA UDI 7f5b55d6-f551-471c-9875-d7cf624c79f8 35 fields · synced Jul 10, 2026
  • EUDAMED 4cc7fdde-9ad8-4988-9eda-fe99e3e20d36 61 fields · synced Jul 10, 2026