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CAMLOG® Titanium base CAD/CAM

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref K2244.3330Ref K2210.5030Ref K2210.5015Ref K2244.5015Ref K2210.4330Ref K2244.5048Ref K2244.5030Ref K2244.4330

by ALTATEC GmbH

Identity

Trade Name
CAMLOG® Titanium base CAD/CAM EUDAMEDFDA UDI
CAMLOG® Titanium base CAD/CAM EUDAMED
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
CAMLOG® Titanium base CAD/CAM EUDAMED
K2244.5048 CAMLOG® Titanium base CAD/CAM d 5.0 mm FDA UDI
Model / Reference
K2244.3330 EUDAMED
K2210.5030 EUDAMED
K2210.5015 EUDAMED
K2244.5015 EUDAMED
K2210.4330 EUDAMED
K2244.5048 EUDAMEDFDA UDI
K2244.5030 EUDAMED
K2244.4330 EUDAMED
Description
K2244.5048 CAMLOG® Titanium base CAD/CAM d 5.0 mm FDA UDI

Identifiers

Catalog Number
K2244.5048 FDA UDI
Primary DI / UDI-DI
04099797017625 EUDAMED
04099797017601 EUDAMED
04099797017595 EUDAMED
04099797017670 EUDAMED
04099797017571 EUDAMED
04099797007060 EUDAMED
04099797017687 EUDAMED
04099797017663 EUDAMED
E219K224450481 FDA UDI
Basic UDI-DI
40997970001113000000000C5 EUDAMED
Secondary DI
E219K224433301 EUDAMED
E219K221050301 EUDAMED
E219K221050151 EUDAMED
E219K224450151 EUDAMED
E219K221043301 EUDAMED
E219K224450481 EUDAMED
E219K224450301 EUDAMED
E219K224443301 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

CAMLOG® Titanium base CAD/CAM 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 (9)

  • EUDAMED d84a5dcd-9568-4cd2-9247-1e1090aa9363 61 fields · synced Jul 26, 2026
  • EUDAMED f832b81d-37ae-463e-a3c5-cd900da54fd5 61 fields · synced May 17, 2026
  • EUDAMED 7b0e8fe1-dc22-485b-ad1b-13f9819aa3c9 61 fields · synced May 17, 2026
  • EUDAMED 367a9a8d-eef2-40b0-94e6-2386ab322043 61 fields · synced May 17, 2026
  • EUDAMED 7dfa0322-97ba-4c4b-a1d2-3710b7334d0e 61 fields · synced May 17, 2026
  • EUDAMED 72597c2e-2536-4bb1-8ac4-235a3766dd7e 61 fields · synced May 18, 2026
  • EUDAMED 5d2b8916-ac8a-42ab-a192-a764235773b5 61 fields · synced May 19, 2026
  • EUDAMED e40fcddf-70ce-403b-adfc-8509c38471b4 61 fields · synced May 19, 2026
  • FDA UDI d20e3052-436c-4aa7-91ad-c76a600fd9cc 36 fields · synced May 30, 2026