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Soldering aid for bar abutment

FDA UDI

Class I (US FDA UDI)

by ALTATEC GmbH

Identity

Trade Name
Soldering aid for bar abutment FDA UDI
Generic Name
Dental implant abutment analog, laboratory FDA UDI
Device Name
Soldering aid for bar abutment Ø 5.0/6.0 mm FDA UDI
Model / Reference
J3020.6000 FDA UDI
Description
Soldering aid for bar abutment Ø 5.0/6.0 mm FDA UDI

Identifiers

Catalog Number
J3020.6000 FDA UDI
Primary DI / UDI-DI
E219J302060001 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant abutment analog, laboratory FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental implant abutment analog, laboratory

Soldering aid for bar abutment by ALTATEC GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant abutment analog, laboratory.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ALTATEC GmbH

Sources (1)

  • FDA UDI c717c1aa-8aab-4e4f-b0b9-87c8d1d03ec3 35 fields · synced May 30, 2026