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CAMLOG® Impression post
EUDAMEDFDA UDIClass I (EU MDR)
Ref K2111.4300
by ALTATEC GmbH
Identity
- Trade Name
- CAMLOG® Impression post EUDAMEDCAMLOG® Impression post PS FDA UDI
- Generic Name
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
- Device Name
- CAMLOG® Impression post, closed tray, sterile EUDAMEDCAMLOG® Impression post PS, closed tray, incl. impression cap, bite registration cap and fixing screw, Ø 4.3 mm, prosthetic height 10.7 mm, titanium alloy/PBT, sterile FDA UDI
- Model / Reference
- K2111.4300 EUDAMEDFDA UDI
- Description
- CAMLOG® Impression post PS, closed tray, incl. impression cap, bite registration cap and fixing screw, Ø 4.3 mm, prosthetic height 10.7 mm, titanium alloy/PBT, sterile FDA UDI
Identifiers
- Catalog Number
- K2111.4300 FDA UDI
- Primary DI / UDI-DI
- 04099797017151 EUDAMEDE219K211143001 FDA UDI
- Basic UDI-DI
- 40997970006002000000000FH EUDAMED
- Secondary DI
- E219K211143001 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 40997970006002000000000FH | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- ALTATEC GmbH
- EUDAMED SRN
- DE-MF-000006230
Sources (2)
- EUDAMED 92aa59f3-3fc6-4de4-b49d-2e9def0c20b7 61 fields · synced Jun 8, 2026
- FDA UDI 8bee9d76-5258-4e33-891a-592c4f79fc4a 35 fields · synced May 29, 2026