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Ena Post CPF0208

by Micerium SpA

Ref CPF0208Model Ena Post Drill

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

CE MDR CE MDD

Valid until

No date given

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number++EMICFAM1C3U3 Basic UDI-DI EMICCPF02081UDI-DIDate26 May 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number++EMICFAM1C3U3 Basic UDI-DI EMICCPF02081UDI-DIDate26 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberEMICCPF02081 UDI-DI Date3 May 2023ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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/MDD, CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Ena Post
Generic name
Dental restoration retention pin
Device name
Name: Ena Post Model: Drill
Ena Post Drill
Model / Ref / Catalog
CPF0208, Ena Post Drill
Description
Ena Post ENAPOST Fiber Post Conicity 2%
Primary DI / UDI-DI
EMICCPF02081
Basic UDI-DI
++EMICFAM1C3U3, B-EMICCPF02081
FDA product code
ELR
EMDN code
L159007 Odontostomatology burs, reusable
GMDN term
Dental restoration retention pin
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.3810
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution
Size
Length — 1.25 Millimeter
Outer Diameter — 0.8 Millimeter

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I
Sterilise before useEUDAMED
No
Yes
GUDID
No
ImplantableEUDAMED
No
GUDID
Yes

Related devices

Category: Dental restoration retention pin

Other devices from Micerium SpA

See all devices from Micerium SpA →

Properties

  • Sterilise before use NoEUDAMEDGUDIDYesEUDAMED
  • Single use
  • Implantable NoEUDAMEDYesGUDID
  • Reprocessed single-use device YesEUDAMEDNoEUDAMED
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date

Other properties (18)

  • Supplied sterile: No
  • Reusable: No
  • Contains latex: No
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
  • Incorporates a substance derived from human blood or plasma: No
  • Contains human tissues or cells: No
  • Contains animal tissues or cells: No
  • Contains endocrine-disrupting substances: No
  • Administering medicine: No
  • Measuring function: No
  • Incorporates a medicinal substance: No
  • Prescription use: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No