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ENDODONTIC POSTS PIVOT tit. EQUATOR mm.7

by Rhein 83 SRL

Ref 336PTE7Model *PERNI EQUATOR

ENDODONTIC POSTS PIVOT tit. EQUATOR mm.7 (336PTE7) is a device classified as Class IIa in the EU and Class I in the US made by Rhein 83 SRL, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-08059224117393) and listed in FDA GUDID since 12 Jul 2021 (UDI-DI 08059224117393), active as of 7 Nov 2026.

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

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 NumberB-08059224117393 Basic UDI-DI 08059224117393UDI-DIDate6 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08059224117393 UDI-DI Date12 Jul 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-08059224117393 registered 6 Nov 2026 Active
  • FDA GUDID UDI-DI 08059224117393 listed 12 Jul 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08059224117393
  2. Registered EUDAMED B-08059224117393

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
PIVOT tit. EQUATOR mm.7 EUDAMED
Endodontic Posts GUDID
Generic name
Dental implant suprastructure, permanent, preformed
Device name
336PTE7
Model / Ref / Catalog
*PERNI EQUATOR, 336PTE7, PIVOT tit. EQUATOR mm.7
Primary DI / UDI-DI
08059224117393
Basic UDI-DI
B-08059224117393
FDA product code
ELR
EMDN code
Q010199 Conservative dentistry and endodontics devices - other
GMDN term
Dental implant suprastructure, permanent, preformed
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.3810
EU registration type
Legacy device (under a directive)
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
*PERNI EQUATOR
336PTE7
GUDID
PIVOT tit. EQUATOR mm.7
Device classEUDAMED
Class IIa
GUDID
Class I
ImplantableEUDAMED
No
GUDID
Yes

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Dental implant suprastructure, permanent, preformed

Similar devices in this category

Other devices filed under CONSERVATIVE DENTISTRY AND ENDODONTICS DEVICES - OTHER.

Other devices from Rhein 83 SRL

See all devices from Rhein 83 SRL →

Properties

  • Sterilise before use
  • Single use
  • Implantable NoEUDAMEDYesGUDID
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (18, all answered No)