- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jun 22, 2026
872076918P01N7Posigo Pelvic Positioning Belt M Side Release is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by The Hague Care Development B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
NL-MF-000027683(01)08720769180738
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.
Read the instructions for use carefully before installation and use. This product must be fitted, and adjusted by a qualified rehabilitation professional.
A loose belt can lead to slipping and strangulation. A detached belt can cause falls or slipping. Always firmly tighten the positioning belt across the pelvis or thigh. This product is not suitable as a vehicle safety belt or to restrict freedom of movement. Not suitable for users who cannot independently release the belt, particularly in emergency situations. Users with limited physical or cognitive abilities require permanent caregiver supervision during use.
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 10 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | — | Still on market |
| Belgium | — | Still on market |
| Germany | — | Still on market |
| Denmark | — | Still on market |
| Spain | — | Still on market |
| Finland | — | Still on market |
| France | — | Still on market |
| Italy | — | Still on market |
| Norway | — | Still on market |
| Sweden | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
08720769180738Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
872076918P01N7P01M-CSID40UDI 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.
Y180980SEATING SYSTEMS / POSTURE SYSTEMS / SEATING AIDS - ACCESSORIESPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →872076918P01N7On the marketPosigo Pelvic Positioning Belt M Pin Buckle872076918P01N7On the marketPosigo Pelvic Positioning Belt M Push Buckle872076918P01N7On the marketPosigo Pelvic Positioning Belt S872076918P01N7On the marketPosigo Pelvic Positioning Belt S FidLock872076918P01N7On the marketPosigo Pelvic Positioning Belt S Pin Buckle872076918P01N7On the marketNo certificate specifically references this device's Basic UDI-DI.
No 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.