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CONELOG® Abutment screw

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref C4004.1601

by ALTATEC GmbH

Identity

Trade Name
CONELOG® Abutment screw EUDAMEDFDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
CONELOG®Abutment screw reduced head EUDAMED
CONELOG® Abutment screw with reduced head, hex, light blue anodized, for Ø 3.3/3.8/4.3 mm, thread M1.6, titanium alloy FDA UDI
Model / Reference
C4004.1601 EUDAMEDFDA UDI
Description
CONELOG® Abutment screw with reduced head, hex, light blue anodized, for Ø 3.3/3.8/4.3 mm, thread M1.6, titanium alloy FDA UDI

Identifiers

Catalog Number
C4004.1601 FDA UDI
Primary DI / UDI-DI
04099797002935 EUDAMED
E219C400416011 FDA UDI
Basic UDI-DI
40997970001502000000000EV EUDAMED
Secondary DI
E219C400416011 EUDAMED
FDA Product Code
NHA FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

CONELOG® Abutment screw by ALTATEC GmbH — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ALTATEC GmbH
EUDAMED SRN
DE-MF-000006230

Sources (2)

  • EUDAMED a3b648b5-8c78-4da6-a93d-04f9d371facd 61 fields · synced Jul 29, 2026
  • FDA UDI aa2793e2-3e7e-4518-a3f8-252c11f10741 35 fields · synced May 30, 2026