← Back to catalogue

Titanium bonding base for CAMLOG® bar abutment

FDA UDIEUDAMED

Class II (US FDA UDI)

by ALTATEC GmbH

Identity

Trade Name
Titanium bonding base for CAMLOG® bar abutment FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
J2260.4300 Titanium bonding base for CAMLOG® bar abutment, Passive-fit Ø 4.3 FDA UDI
Model / Reference
J2260.4300 FDA UDI
Description
J2260.4300 Titanium bonding base for CAMLOG® bar abutment, Passive-fit Ø 4.3 FDA UDI

Identifiers

Catalog Number
J2260.4300 FDA UDI
Primary DI / UDI-DI
E219J226043001 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

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

Titanium bonding base for CAMLOG® bar abutment by ALTATEC GmbH — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
ALTATEC GmbH

Sources (2)

  • FDA UDI 0168bb1c-5e9a-4e71-be02-4443bd4b6e39 36 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced May 29, 2026