← Back to catalogue

Neoss Implant System

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 51160

by Neoss, Ltd.

Identity

Trade Name
Neoss® Guide - Drill-Hub I EUDAMED
Neoss Implant System FDA UDI
Generic Name
Fixture/appliance dental drill bit, single-use FDA UDI
Device Name
Handpiece connection instrument EUDAMED
Neoss® Guide - Drill-Hub I FDA UDI
Model / Reference
51160 EUDAMEDFDA UDI
Description
Neoss® Guide - Drill-Hub I FDA UDI

Identifiers

Catalog Number
51160 FDA UDI
Primary DI / UDI-DI
05060440332715 EUDAMEDFDA UDI
Basic UDI-DI
506044033N0035N4 EUDAMED
Direct Marketing DI
05060440332715 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Fixture/appliance dental drill bit, single-use 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

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: Fixture/appliance dental drill bit, single-use

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 Fixture/appliance dental drill bit, single-use.

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

Manufacturer
Neoss, Ltd.

Sources (2)

  • FDA UDI 83740779-9ad4-41b0-8b4e-84e30fc5de03 35 fields · synced Aug 2, 2026
  • EUDAMED a2bf6bde-40b2-4a74-ac7f-19a1d2dc9d7d 61 fields · synced Aug 2, 2026