- Role
- Country
- Date of registration
- Address
PL-MF-000052302Nóż sekcyjny typu VIRCHOW, dł. całk. 385 mm, dł. ostrza 240 mm is an MDD-legacy medical device registered in EUDAMED. It is classified as Class I. Manufactured by Fabryka Narzędzi Medycznych Chirmed Marcin Dyner Spółka Komandytowa. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Mar 17, 2026
B-05904151404135Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)05904151404135
1 warning recorded — scroll inside the panel to see all entries.
CW129Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Poland; available across 1 country total.
Placed on the market in Poland; per-country availability dates not published.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
05904151404135Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-05904151404135CO 306UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
European Medical Device Nomenclature — the EU product classification assigned to this device.
L010101MONOBLOCK SURGICAL SCALPELS, REUSABLENo certificate specifically references this device's Basic UDI-DI.
B-05904151414424On the marketMirror handle, solid59041514MH01JJOn the marketMyofical release of soft tissue instrument59041514RI01KSOn the marketOrthodontic forceps 130 mm59041514FC03GCOn the marketOrthodontic mirror59041514DM01HCOn the marketParallel implant placement systemB-05904151421491On the marketNo certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.