- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Feb 10, 2023
4030155KaWe03SNF.O. battery-/charging handle, medium, 2.5 V is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Kirchner & Wilhelm GmbH + Co KG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0403015500909803.41000.721DE-MF-000006338No certificate specifically references this device's Basic UDI-DI.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →(01)04030155009098
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
2 warnings recorded — scroll inside the panel to see all entries.
Sterile
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 Germany; available across 1 country total.
Placed on the market in Germany; per-country availability dates not published.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12021003LARYNGOSCOPESPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →Certificate health across this manufacturer's portfolio.
MDR-002IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →4030155KaWe0101YROn the marketF.O. battery handle, large, 2.5 V4030155KaWe03SNOn the marketF.O. battery handle, short, 2.5 V4030155KaWe03SNOn the marketF.O. battery-/charging handle, medium, incl. NiMH accu, 2.5 V4030155KaWe03SNOn the marketF.O. battery-/charging handle, small, 2.5 V4030155KaWe03SNOn the marketF.O. charging handle, medium, incl. Li-Ion accu, 3.5 V4030155KaWe03SNOn the market