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Ena Post CPF0210

by Micerium SpA

Ref CPF0210Model Ena Post Drill

Ena Post CPF0210 is a device classified as Class IIa in the EU and Class I in the US made by Micerium SpA, registered in EUDAMED on 26 May 2026 (Basic UDI-DI ++EMICFAM1C3U3) and listed in FDA GUDID since 3 May 2023 (UDI-DI EMICCPF02101), active as of 7 Nov 2026.

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

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number++EMICFAM1C3U3 Basic UDI-DI EMICCPF02101UDI-DIDate26 May 2026RegisteredStatusActive
European UnionCE/MDR EUDAMED Number++EMICFAM1C3U3 Basic UDI-DI EMICCPF02101UDI-DIDate26 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberEMICCPF02101 UDI-DI Date3 May 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++EMICFAM1C3U3 registered 26 May 2026 Active· +1 more in the status table
  • FDA GUDID UDI-DI EMICCPF02101 listed 3 May 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID EMICCPF02101
  2. Registered EUDAMED ++EMICFAM1C3U3

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  • Withdrawn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
CPF0210, Ena Post Drill
Description
Ena Post ENAPOST Fiber Post Conicity 2%
Primary DI / UDI-DI
EMICCPF02101
Basic UDI-DI
++EMICFAM1C3U3, B-EMICCPF02101
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
Outer Diameter — 1.0 Millimeter
Length — 1.45 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, all answered No)