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Errecieffe srl

Italy·IT-MF-000017627

Last updated September 18, 2026

What Errecieffe srl makes

Errecieffe srl manufactures dental and orthopedic tools, including analogue screws, abutments for dental implants (both castable and CR-CO variants), and dental drills with countersinks and stop mechanisms. Their portfolio also covers specialized tools for garbaggio (bone grafting) procedures, screwdrivers, cover screws, and taps for orthopedic applications, as well as a scanning device referred to as SCAN BODY for medical imaging purposes.

The company’s devices are classified under EU regulations as Class I, Class IIa, and Class IIb, with all products registered in the EU’s eudamed database. The manufacturer is based in Italy and adheres to EU medical device compliance requirements for their listed products.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Errecieffe srl manufacture?

Errecieffe srl manufactures dental and orthopedic tools including analogue screws, abutments for dental implants (both castable and CR-CO variants), dental drills with countersinks and stop mechanisms, specialized tools for bone grafting procedures, screwdrivers, cover screws, taps for orthopedic applications, and a scanning device called SCAN BODY for medical imaging purposes.

Where is Errecieffe srl based?

Errecieffe srl is based in Italy, as indicated by the country code IT in their device registration information.

Which regulatory registries list Errecieffe srl's devices?

Errecieffe srl's devices are listed in the EU's eudamed database, which is the European database for medical devices. This registry contains information about medical devices that are compliant with EU regulations.

How are Errecieffe srl's devices classified?

Errecieffe srl's devices are classified under EU regulations into three categories: Class I, Class IIa, and Class IIb. These classifications indicate the level of risk associated with each device, with Class I being the lowest risk and Class IIb being higher risk devices that require more stringent regulatory controls.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Italy
Address
68, Via Vittorio Emanuele II, Ponte San Pietro, Italy
LinkedIn
—
Facebook
—
Phone
+39 3405181203
PRRC Contact
Selene Agliati
EUDAMED SRN
IT-MF-000017627
FDA FEI Number
—
DUNS Number
—

Catalogue (17)

DeviceModel / ReferenceRegistriesClassStatus
Scan Body SCAN-MPI
EUDAMED
Class IActive
Tools For Garbaccio 011
EUDAMED
Class IActive
Analogue AND-MPI
EUDAMED
Class IActive
Fixos FX20350125
EUDAMED
Class IActive
Screw For Analogues Z-VAND-I
EUDAMED
Class IActive
Transfer TR-MPI
EUDAMED
Class IActive
Castable Abutment MCE-MPI
EUDAMED
Class IActive
Dental Drill, Countersink, Stop FRLI
EUDAMED
Class IIaActive
Cr-Co Abutments MCRE-MPI
EUDAMED
Class IIbActive
Screwdrivers And Tools CAC-I
EUDAMED
Class IIaActive
Cover Screw CSMP-I
EUDAMED
Class IIbActive
Taps MAS-33
EUDAMED
Class IIaActive
Fresa Per Zigomatico FR12-S
EUDAMED
Class IIaActive
Gold Abutment MGE-MPE
EUDAMED
Class IIbActive
Frese Per Impianto Pterigoideo FR2024L
EUDAMED
Class IIaActive
Osteotome OST2
EUDAMED
Class IIaActive
Mucotome MUC45
EUDAMED
Class IIaActive

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