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Neoss Implant System

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 41151

by Neoss, Ltd.

Identity

Trade Name
Surgical Instrument Kit EUDAMED
Neoss Implant System FDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Reusable Drill EUDAMED
Surgical Instrument Kit FDA UDI
Model / Reference
41151 EUDAMEDFDA UDI
Description
Surgical Instrument Kit FDA UDI

Identifiers

Catalog Number
41151 FDA UDI
Primary DI / UDI-DI
05060440332494 EUDAMEDFDA UDI
Basic UDI-DI
506044033N0016MY EUDAMED
Direct Marketing DI
05060440332494 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Dental/maxillofacial surgical procedure kit, non-medicated, 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

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, reusableDental/maxillofacial surgical procedure kit, non-medicated, 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 Dental/maxillofacial surgical procedure kit, non-medicated, 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 f5587154-f37c-4695-9f6c-8f5192f030aa 35 fields · synced Jun 19, 2026
  • EUDAMED dff178de-8fc0-47b4-a7be-c291a2619356 61 fields · synced Jun 19, 2026