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Titanium cap

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref J2259.6001

by ALTATEC GmbH

Identity

Trade Name
Titanium cap EUDAMED
Titanium cap for crown for bar abutment FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Prosthetic Parts EUDAMED
Titanium cap for crown for bar abutment, incl. prosthetic screw, light blue anodized, for bar abutments Ø 5.0/6.0 mm, titanium alloy FDA UDI
Model / Reference
J2259.6001 EUDAMEDFDA UDI
Description
Titanium cap for crown for bar abutment, incl. prosthetic screw, light blue anodized, for bar abutments Ø 5.0/6.0 mm, titanium alloy FDA UDI

Identifiers

Catalog Number
J2259.6001 FDA UDI
Primary DI / UDI-DI
04099797003925 EUDAMED
E219J225960011 FDA UDI
Basic UDI-DI
40997970004502000000000JQ EUDAMED
Secondary DI
E219J225960011 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 IIa 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

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

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

Titanium cap by ALTATEC GmbH — Class IIa — 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 ce7d1f5e-e216-48ac-aa13-0de83c3698db 61 fields · synced Jul 17, 2026
  • FDA UDI 34d9c07f-57fa-4cb6-895e-65ccaa49491c 35 fields · synced May 25, 2026