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CAMLOG® Impression post

EUDAMEDFDA UDI

Class I (EU MDR)

Ref K2114.3800

by ALTATEC GmbH

Identity

Trade Name
CAMLOG® Impression post EUDAMED
CAMLOG® Impression post FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
CAMLOG® Impression post, closed tray, sterile EUDAMED
CAMLOG® Impression post, wide body, closed tray, incl. impression cap, bite registration cap and fixing screw, Ø 3.8 mm, prosthetic height 10.7 mm, titanium alloy/PBT, sterile FDA UDI
Model / Reference
K2114.3800 EUDAMEDFDA UDI
Description
CAMLOG® Impression post, wide body, closed tray, incl. impression cap, bite registration cap and fixing screw, Ø 3.8 mm, prosthetic height 10.7 mm, titanium alloy/PBT, sterile FDA UDI

Identifiers

Catalog Number
K2114.3800 FDA UDI
Primary DI / UDI-DI
04099797017205 EUDAMED
E219K211438001 FDA UDI
Basic UDI-DI
40997970006002000000000FH EUDAMED
Secondary DI
E219K211438001 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

CAMLOG® Impression post by ALTATEC GmbH — Class I — 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 4e31370b-b454-4fd8-9494-f44a25ba94ca 61 fields · synced Aug 4, 2026
  • FDA UDI 387dd568-f925-46dd-982f-5ae426d1baff 35 fields · synced May 30, 2026