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JP-MF-000007213Body Comp Monitor BF511 Blue (HBF-511B-E) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by OMRON Healthcare Co., Ltd.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jul 12, 2023
4015672104054UPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)04015672104051
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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 Netherlands; available across 28 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Jan 1, 2023 | Jan 1, 2028 |
| Belgium | Jan 1, 2023 | Jan 1, 2028 |
| Bulgaria | Jan 1, 2023 | Jan 1, 2028 |
| Cyprus | Jan 1, 2023 | Jan 1, 2028 |
| Czechia | Jan 1, 2023 | Jan 1, 2028 |
| Germany | Jan 1, 2023 | Jan 1, 2028 |
| Denmark | Jan 1, 2023 | Jan 1, 2028 |
| Estonia | Jan 1, 2023 | Jan 1, 2028 |
| EL | Jan 1, 2023 | Jan 1, 2028 |
| Spain | Jan 1, 2023 | Jan 1, 2028 |
| Finland | Jan 1, 2023 | Jan 1, 2028 |
| France | Jan 1, 2023 | Jan 1, 2028 |
| Croatia | Jan 1, 2023 | Jan 1, 2028 |
| Hungary | Jan 1, 2023 | Jan 1, 2028 |
| Ireland | Jan 1, 2023 | Jan 1, 2028 |
| Iceland | Jan 1, 2023 | Jan 1, 2028 |
| Italy | Jan 1, 2023 | Jan 1, 2028 |
| Lithuania | Jan 1, 2023 | Jan 1, 2028 |
| Luxembourg | Jan 1, 2023 | Jan 1, 2028 |
| Latvia | Jan 1, 2023 | Jan 1, 2028 |
| Poland | Jan 1, 2023 | Jan 1, 2028 |
| Portugal | Jan 1, 2023 | Jan 1, 2028 |
| Romania | Jan 1, 2023 | Jan 1, 2028 |
| Sweden | Jan 1, 2023 | Jan 1, 2028 |
| Slovenia | Jan 1, 2023 | Jan 1, 2028 |
| Slovakia | Jan 1, 2023 | Jan 1, 2028 |
| Türkiye | Jan 1, 2023 | Jan 1, 2028 |
| XI | Jan 1, 2023 | Jan 1, 2028 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
04015672104051Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
4015672104054UHBF-511B-EUDI 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.
Z12099001BODY IMPEDANCE ANALYSERSCertificate health across this manufacturer's portfolio.
HZ 2102042-1ReissuedHZ 2102042-1SupplementedNotified 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 →4015672102424QOn the marketBF212 (HBF-212-EW)40156721070357On the marketBF214 (HBF-214-EBW)40156721070459On the marketBody Comp Monitor BF511 Turq (HBF-511T-E)4015672104064WOn the marketC30-2-UK (C30-UK-AC)4015672112845FOn the marketC30-E-AC (C30-2-E)4015672112835DOn the marketNo certificate specifically references this device's Basic UDI-DI.