- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Apr 28, 2026
B-04260125710246Silverline® Ventricular Drainage Catheter with Cranial Bolt 8F is an MDD-legacy medical device registered in EUDAMED. It is classified as Class III. Manufactured by Spiegelberg GmbH & Co. KG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
04260125710246EVD30.014.02DE-MF-000000008170772620(01)04260125710246
1 warning recorded — scroll inside the panel to see all entries.
CW010Sterile
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.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jul 1, 2024 | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
N010303CEREBRAL FLUID EXTERNAL DRAINS AND KITSA0601010201DRAINAGE SYSTEMS WITH ADJUSTABLE SUCTION AND COLLECTION CHAMBERPrimary 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 →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 →B-04260125710307On the marketSilverline® Ventricular Drainage Catheter 8FB-04260125710185On the marketSilverline® Ventricular Drainage Catheter with Cranial Bolt 10FB-04260125713025On the marketSilverline® Ventricular Probe 10FB-04260125712561On the marketSilverline® Ventricular Probe 8FB-04260125712554On the marketSilverline® Ventricular Probe with Cranial Bolt 8FB-04260125712905On the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
1000265927Issued1000265951Issued1000216002Issued1000210544IssuedNotified 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 →Notified 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 →Notified 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 →Notified 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 →