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CAMLOG® Connection Reamer

by ALTATEC GmbH 4 variants

Ref K5901.3300

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number40997970006806000000000UD Basic UDI-DI 04099797018936UDI-DIDate1 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04099797018936 UDI-DI Date10 Feb 2026ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
CAMLOG® Connection Reamer EUDAMEDGUDID
CAMLOG® Connection Reamer Set GUDID
Generic Name
Dental implant extractor
Model / Ref / Catalog
K5901.3300
Primary DI / UDI-DI
04099797018936, E219K590133001
Basic UDI-DI
40997970006806000000000UD
Secondary DI
E219K590133001
FDA Product Code
NDP
EMDN Code
Z12110180 Instruments for dental treatment units - hardware accessories
GMDN Term
Dental implant extractor
Device Class
Class I
Regulation Number
872.3980
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 3.3 Millimeter

Manufacturer details

EUDAMED SRN
DE-MF-000006230

Other devices from ALTATEC GmbH

See all devices from ALTATEC GmbH →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (17)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No