- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Mar 27, 2026
B-58888483001618JMS Transfusion Set is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by JMS Singapore Pte Ltd. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
58888483001618812-0204(01)58888483001618
European Medical Device Nomenclature — the EU product classification assigned to this device.
B99HAEMATOLOGY AND HAEMOTRANSFUSION DEVICES - OTHER3 warnings recorded — scroll inside the panel to see all entries.
Primary placement in Germany; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
| Sweden | — | Still on market |
SG-MF-000024704G1 027106 0064Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →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.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
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 →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 →Certificate health across this manufacturer's portfolio.
G15 027106 0070SupplementedNotified 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 →B-58888483001830On the marketJMS Transfer BagB-58888483005043On the marketJMS Transfusion SetB-58888483000130On the marketPlume SP MINI A.V. Fistula Needle SetB-58888483003186On the marketPlume SP MINI A.V. Fistula Needle SetB-58888483003087On the marketPlume SP MINI A.V. Fistula Needle SetB-58888483003230On the marketNo certificate specifically references this device's Basic UDI-DI.