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Laboratory

EUDAMED

Class IIb (EU MDR)

Ref 260-650-600Ref 260-650-605

by Bicon, LLC

Identity

Trade Name
Laboratory EUDAMED
Device Name
Dental Abutment EUDAMED
Model / Reference
260-650-600 EUDAMED
260-650-605 EUDAMED

Identifiers

Primary DI / UDI-DI
00813110025425 EUDAMED
00813110025432 EUDAMED
Basic UDI-DI
B-00813110025425 EUDAMED
B-00813110025432 EUDAMED
EMDN Code
P010299 ODONTOLOGICAL PROSTHESES - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Category: Dental implant suprastructure, permanent, preformed

Laboratory by Bicon, Llc — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Bicon, LLC
EUDAMED SRN
US-MF-000002782
Authorised Representative
Bicon Europe Ltd IE-AR-000002497

Sources (2)

  • EUDAMED 9123cb99-867e-4ed8-9371-837dd77d55c0 61 fields · synced Jul 20, 2026
  • EUDAMED d0efcb10-403e-4312-b161-ab0c676694b1 61 fields · synced May 19, 2026