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WILDmedical GmbH

Germany·DE-MF-000017096

Last updated September 17, 2026

What WILDmedical GmbH makes

Wildmedical GmbH manufactures reusable surgical instruments, including fluted drill bits, enucleation scissors, nasal saws, Liston amputation knives, hollow chisels, iris scissors, dissecting scalpels, screwdrivers, scalpel handles, ear forceps, and osteotomes.

These devices are classified as Class I under EU regulations and are registered in the eudamed database. The company is based in Germany.

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

Frequently asked questions

What types of medical devices does Wildmedical GmbH manufacture?

Wildmedical GmbH specializes in reusable surgical instruments, primarily focusing on Class I devices. Their product range includes fluted surgical drill bits, enucleation scissors, nasal saws, Liston amputation knives, hollow chisels, iris scissors, dissecting scalpels, screwdrivers, scalpel handles, ear forceps, and osteotomes. These tools are designed for surgical procedures and are intended for single-use or repeated use in controlled environments.

Where is Wildmedical GmbH based, and what is its primary focus?

Wildmedical GmbH is based in Germany. The company’s primary focus is on manufacturing reusable surgical instruments, particularly those used in precision surgical applications. Their devices are tailored for medical professionals performing procedures requiring specialized tools, such as ophthalmic, orthopedic, or ENT (ear, nose, and throat) surgeries.

Which regulatory registries list Wildmedical GmbH’s devices?

Wildmedical GmbH’s devices are listed in the eudamed database, which is the European Union’s central registry for medical devices. This registry ensures transparency and traceability of devices authorized under EU regulations, allowing healthcare providers, regulators, and other stakeholders to verify the presence of these instruments in the market.

How are Wildmedical GmbH’s devices classified under EU regulations?

Wildmedical GmbH’s devices are classified as Class I under EU medical device regulations. This classification applies to low-risk instruments, such as reusable surgical tools like drills, scissors, and scalpels, which pose minimal risk to patients when used as intended. Class I devices typically undergo basic requirements for safety and performance but do not require a full conformity assessment process.

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

Information

Country
Germany
Address
18, Ehrenbergstr. , Tuttlingen, Germany
LinkedIn
—
Facebook
—
Phone
—
PRRC Contact
Nicole Menean
EUDAMED SRN
DE-MF-000017096
FDA FEI Number
3015451162
DUNS Number
—

Catalogue (11)

DeviceModel / ReferenceRegistriesClassStatus
Drill MW01.204.20
EUDAMED
Class IActive
Enukleationsschere MW16.386.13
EUDAMED
Class IActive
Nasen Säge MW42.295.19
EUDAMED
Class IActive
LISTON Amputationsmesser MW08.530.13
EUDAMED
Class IActive
Hohlmeisselzange MW28.490.01
EUDAMED
Class IActive
IRIS Schere MW16.350.09
EUDAMED
Class IActive
DISSECTING Skalpell MW08.502.01
EUDAMED
Class IActive
Schraubendreher MW01.203.00
EUDAMED
Class IActive
Skalpellgriff MW08.200.04
EUDAMED
Class IActive
Ohrzängchen MW42.495.08
EUDAMED
Class IActive
Osteotom MW28.200.02
EUDAMED
Class IActive

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