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CONELOG® PROGRESSIVE-LINE Implant

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref C1086.4311

by ALTATEC GmbH

Identity

Trade Name
CONELOG® PROGRESSIVE-LINE Implant EUDAMED
CONELOG® PROGRESSIVE-LINE Implant, Promote® plus FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
CONELOG® Progressive-Line Implant EUDAMED
CONELOG® PROGRESSIVE-LINE Implant, Promote® plus, d 4.3 mm, L 11 mm FDA UDI
Model / Reference
C1086.4311 EUDAMEDFDA UDI
Description
CONELOG® PROGRESSIVE-LINE Implant, Promote® plus, d 4.3 mm, L 11 mm FDA UDI

Identifiers

Catalog Number
C1086.4311 FDA UDI
Primary DI / UDI-DI
04099797008128 EUDAMED
E219C108643111 FDA UDI
Basic UDI-DI
40997970000302000000000BA EUDAMED
Secondary DI
E219C108643111 EUDAMED
FDA Product Code
DZE FDA UDI
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED
GMDN Term
Screw endosteal dental implant, two-piece FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 4.3 Millimeter FDA UDI
Length — 11 Millimeter FDA UDI

CONELOG® PROGRESSIVE-LINE Implant 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 4b906b71-861e-4180-8f46-22e20138d92c 61 fields · synced Sep 18, 2026
  • FDA UDI 81abfda5-370e-4166-aa6a-82318ac22080 36 fields · synced May 30, 2026