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CONELOG® CAM Titanium Blank

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref C2471.4327Ref C2471.3327Ref C2442.5020

by ALTATEC GmbH

Identity

Trade Name
CONELOG® CAM Titanium Blank EUDAMED
CONELOG® CAM Titan. Blank, type ME FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
CONELOG® CAM Titanium Blank EUDAMED
CONELOG® CAM Titan. Blank, type ME, d 12 mm, d 5.0 mm, L 20.0 mm, 10 units FDA UDI
Model / Reference
C2471.4327 EUDAMED
C2471.3327 EUDAMED
C2442.5020 EUDAMEDFDA UDI
Description
CONELOG® CAM Titan. Blank, type ME, d 12 mm, d 5.0 mm, L 20.0 mm, 10 units FDA UDI

Identifiers

Catalog Number
C2442.5020 FDA UDI
Primary DI / UDI-DI
04099797007619 EUDAMED
04099797007596 EUDAMED
04099797008753 EUDAMED
E219C244250201 FDA UDI
Basic UDI-DI
40997970001516000000000KG EUDAMED
Secondary DI
E219C247143271 EUDAMED
E219C247133271 EUDAMED
E219C244250201 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
MRI Safety
MR Conditional FDA UDI

CONELOG® CAM Titanium Blank 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
ALTATEC GmbH
EUDAMED SRN
DE-MF-000006230

Sources (4)

  • EUDAMED 02a36fcf-7617-4e31-a2a6-94b762f1f66a 61 fields · synced Jul 28, 2026
  • EUDAMED ab814353-e660-4241-9505-b41876cfdc30 61 fields · synced May 18, 2026
  • EUDAMED db2889ec-42db-43aa-9315-3b7e9f02d979 61 fields · synced May 18, 2026
  • FDA UDI bb0858eb-e181-4e04-8487-fe208cce2597 35 fields · synced May 27, 2026