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CAMLOG® Impression post PS

FDA UDIEUDAMED

Class I (US FDA UDI)

by ALTATEC GmbH

Identity

Trade Name
CAMLOG® Impression post PS FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
CAMLOG® Impression post PS, closed tray d 4.3 mm FDA UDI
Model / Reference
K2109.4300 FDA UDI
Description
CAMLOG® Impression post PS, closed tray d 4.3 mm FDA UDI

Identifiers

Catalog Number
K2109.4300 FDA UDI
Primary DI / UDI-DI
E219K210943001 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use 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

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

Yes

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

Category: Dental implant suprastructure, temporary, preformed, single-use

CAMLOG® Impression post PS by ALTATEC GmbH — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ALTATEC GmbH

Sources (2)

  • FDA UDI ecca74c1-7297-4917-a0d4-9048b799ac1b 35 fields · synced Jun 20, 2026
  • EUDAMED 1 fields · synced May 28, 2026