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Neoss Implant System

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 51171

by Neoss, Ltd.

Identity

Trade Name
Neoss® Guide - Countersink Conduit Ø5.0 EUDAMED
Neoss Implant System FDA UDI
Generic Name
Fixture/appliance dental drill bit, single-use FDA UDI
Device Name
Guide Accessories EUDAMED
Neoss® Guide - Countersink Conduit Ø5.0 FDA UDI
Model / Reference
51171 EUDAMEDFDA UDI
Description
Neoss® Guide - Countersink Conduit Ø5.0 FDA UDI

Identifiers

Catalog Number
51171 FDA UDI
Primary DI / UDI-DI
05060440332807 EUDAMEDFDA UDI
Basic UDI-DI
506044033N0025MZ EUDAMED
Direct Marketing DI
05060440332807 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 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

No

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

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Manufacturer

Manufacturer
Neoss, Ltd.

Sources (2)

  • FDA UDI 3bb247eb-346d-4c51-9b8d-87e2997f7ec7 35 fields · synced Jun 14, 2026
  • EUDAMED 057aba41-736e-419a-8df4-9152389dac74 61 fields · synced Jun 11, 2026