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Neoss Implant System

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 41241

by Neoss, Ltd.

Identity

Trade Name
Bone Remover Cover Screw, NP EUDAMED
Neoss Implant System FDA UDI
Generic Name
Fixture/appliance dental drill bit, reusable FDA UDI
Device Name
Reusable Drill EUDAMED
Bone Remover Cover Screw, NP FDA UDI
Model / Reference
41241 EUDAMEDFDA UDI
Description
Bone Remover Cover Screw, NP FDA UDI

Identifiers

Catalog Number
41241 FDA UDI
Primary DI / UDI-DI
05060440335334 EUDAMEDFDA UDI
Basic UDI-DI
506044033N0016MY EUDAMED
Direct Marketing DI
05060440335334 EUDAMED
FDA Product Code
DZI FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Fixture/appliance dental drill bit, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.4120 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fixture/appliance dental drill bit, reusable

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

Similar devices

Also classified as Fixture/appliance dental drill bit, 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 8e95e001-1e4c-45c1-a176-8c591cf2f17b 34 fields · synced Jun 14, 2026
  • EUDAMED b280f4cd-6980-47f1-a8ff-1796bec13e37 61 fields · synced Jun 11, 2026