← Back to catalogue

Polishing protection

FDA UDI

Class I (US FDA UDI)

by ALTATEC GmbH

Identity

Trade Name
Polishing protection FDA UDI
Generic Name
Dental implant abutment analog, laboratory FDA UDI
Device Name
Polishing protection for caps a. bases f. bar abutm. d 3.3/3.8/4.3 mm FDA UDI
Model / Reference
J3021.4300 FDA UDI
Description
Polishing protection for caps a. bases f. bar abutm. d 3.3/3.8/4.3 mm FDA UDI

Identifiers

Catalog Number
J3021.4300 FDA UDI
Primary DI / UDI-DI
E219J302143001 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

Polishing protection 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

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

Manufacturer

Manufacturer
ALTATEC GmbH

Sources (1)

  • FDA UDI a58f5c75-862f-486e-9ef3-f526dc7f73a2 35 fields · synced May 30, 2026