- Organization name
- UDI-DI code
- Reference / catalog number
ES-MF-000001922AUTOMATIC LOADING SYSTEM PB-440 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Productos metálicos del Bages (Promeba). Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Feb 1, 2023
8437021314seriePB-460VDPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)08436601870278
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 Spain; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Jan 1, 2017 | Dec 31, 2049 |
| Austria | Jan 1, 2017 | Dec 31, 2049 |
| Belgium | Jan 1, 2017 | Dec 31, 2049 |
| Bulgaria | Jan 1, 2017 | Dec 31, 2049 |
| Cyprus | Jan 1, 2017 | Dec 31, 2049 |
| Czechia | Jan 1, 2017 | Dec 31, 2049 |
| Germany | Jan 1, 2017 | Dec 31, 2049 |
| Denmark | Jan 1, 2017 | Dec 31, 2049 |
| Estonia | Jan 1, 2017 | Dec 31, 2049 |
| EL | Jan 1, 2017 | Dec 31, 2049 |
| Finland | Jan 1, 2017 | Dec 31, 2049 |
| France | Jan 1, 2017 | Dec 31, 2049 |
| Croatia | Jan 1, 2017 | Dec 31, 2049 |
| Hungary | Jan 1, 2017 | Dec 31, 2049 |
| Ireland | Jan 1, 2017 | Dec 31, 2049 |
| Iceland | Jan 1, 2017 | Dec 31, 2049 |
| Italy | Jan 1, 2017 | Dec 31, 2049 |
| Liechtenstein | Jan 1, 2017 | Dec 31, 2049 |
| Lithuania | Jan 1, 2017 | Dec 31, 2049 |
| Luxembourg | Jan 1, 2017 | Dec 31, 2049 |
| Latvia | Jan 1, 2017 | Dec 31, 2049 |
| Malta | Jan 1, 2017 | Dec 31, 2049 |
| Netherlands | Jan 1, 2017 | Dec 31, 2049 |
| Norway | Jan 1, 2017 | Dec 31, 2049 |
| Poland | Jan 1, 2017 | Dec 31, 2049 |
| Portugal | Jan 1, 2017 | Dec 31, 2049 |
| Romania | Jan 1, 2017 | Dec 31, 2049 |
| Sweden | Jan 1, 2017 | Dec 31, 2049 |
| Slovenia | Jan 1, 2017 | Dec 31, 2049 |
| Slovakia | Jan 1, 2017 | Dec 31, 2049 |
| Türkiye | Jan 1, 2017 | Dec 31, 2049 |
| XI | Jan 1, 2017 | Dec 31, 2049 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
08436601870278Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
8437021314seriePB-460VDPB4402-00000UDI 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.
V0805038001RIGID SUPPORTS FOR LIFTS (STRETCHERS)No certificate specifically references this device's Basic UDI-DI.
8437021314seriePC-900VXOn the marketAMBULANCE STRETCHER PC-952 FOWLER8437021314seriePC-900VXOn the marketAMBULANCE STRETCHER SET PC-610/7 STD YELLOW8437021314seriePC-600VGOn the marketBASIC PLANE STRETCHER SUPPORT PB-420-38437021314seriePB-420UZOn the marketBASIC STRETCHER SUPPORT BOB FIXED 018437021314seriePB-420UZOn the marketBASIC STRETCHER SUPPORT BOB FIXED 028437021314seriePB-420UZOn 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.