Scire se surgere antequam stent

Quomodo Operatur

Prae-Exitus Detectio, Non Post-Exitus Alarma

Vetusta infirmitas alarmorum exitus est quod pulvillus qui solum sedem vacuam indicat personale nullum tempus ad residentem attingendum praebet. Nostri pulvilli in initio motus ad standum activantur.

TRIGGER PER MUTATIONEM ONERIS

Limis alarmi super cadentem onus, non super onus nullum, constituitur. Inclinatio ante in bracchia iam eum transgreditur.

DIFFERENTIA ADJUSTABILIS

Fenestra confirmationis 0–5 s alarmos vanos ex mutatio positionis supprimit, dum utili antecaput servatur.

SUPERVISIO CONTINUITATIS

Pulvillus disiunctus aut defectus se ipsum indicat. Alarma tacita peior est quam nulla alarma.

Una Plataforma, Omnes Superficies Sedentium

Pulvilli sedentium pro cathedris rotatis, cathedris brachiatis et divanis; pulvilli longi pro lectis curativis. Idem connexio et signi comportamentum per totam seriem, ita ut institutum unum tantum typum monitoris habeat.

Praesidium Exitus Sensorius

Vinyl pad sealed and easy to clean, for wheelchair seats, armchairs, and sofas. Bilingual face print with orientation arrow so caregivers cannot install it upside down.

• 25 x 30 cm active area

• Bilingual EN / ES face print

• Single-key white connector

BED EXIT PAD + MONITOR KIT

Long-format under-sheet pad supplied with alarm monitor. Printed face shows four-step setup instructions and a dated replacement reminder field.

• 25 x 90 cm long format

• Upper-body or waistline placement

• Monitor kit included

BUILT FOR VOLUME SUPPLY

Pads are produced in matched batches with consistent trigger threshold, cable length and connector keying, so a facility can swap any pad into any monitor without recalibration.

• Batch-matched trigger threshold

• Custom cable length and connector

• Private-label face printing

• Annual replacement programme support

Four Ways To Raise The Alert

The pad is the sensing layer. Where the alert lands is your decision — local sounder, existing nurse-call wiring, wireless pager or your own gateway and dashboard.

Specification Overview

Baseline configuration shown; size, threshold, cable length, connector and face artwork are customised per project.

Riesgo de salida de silla y riesgo de salida de cama, un solo proveedor

La salida de la silla es el riesgo diurno; la salida de la cama es el riesgo nocturno. Las instalaciones que adquieren ambos productos de una sola fuente obtienen un comportamiento coherente y un único ciclo de reemplazo.

01SILLA DE RUEDAS Y SALA DIURNA

Una almohadilla de asiento alerta al personal en el instante en que un residente comienza a levantarse de la silla de ruedas, apoyando la supervisión sin necesidad de restricción física.

• Se adapta a cojines de asiento estándar

• Enfoque sin restricciones

• Monitor clips to frame

02CARE BED, NIGHT SHIFT

The long bed pad sits under the sheet at waist or upper-body level, giving the night nurse warning before the resident reaches the floor.

• Under-sheet placement

• Two sensitivity positions

• Nurse-call integration

03HOME CARE & FAMILY

A sofa or armchair pad lets a family carer step into the kitchen without losing awareness of an at-risk parent.

04REHAB & CLINIC SEATING

Waiting-area and therapy chairs are fitted so unsupervised transfer attempts are flagged before they become incidents.

Hermetice clausum, probatum, per partem coniunctum

Cuspidines per radiofrequentiam (RF) in totum hermeticum vinilicum involucrum coniunguntur, deinde in pressu mechanico cycli probantur antequam implicantur. Cuspis quae in repetibilitate liminis deficiat numquam ex linea egreditur.

CONIUNCTIO PER RADIOFREQUENTIAM (RF) AD MARGINEM

Totum hermeticum vinilicum involucrum sine sutura stichata

CALIBRATIO LIMINIS

Omnis pars ad onus activationis praefinitum verificatur

Examinatio cyclorum

Validatio repetibilitatis per pressum mechanicum

ULTIMUM EXAMEN CONTINUATIONIS

Cavea, connexio et cuspis ante implicantionem probantur

Built To Medical Device Standards

Fabricatum sub systemate gestionis qualitatis pro instrumentis medicis, cum materialibus biocompatibilibus ad cutem contrectanda et cum plena documentazione de conformitate substantiarum pro mercatis Europaei et Americani.

ISO 13485:2016

Medical QMS

ISO 10993

Compatibilitas biologica

RoHS / REACH

Substance Compliance

Documenta certificationis et conformitatis emittuntur pro singulis ambitibus operum et praebentur dum recensio technica fit.

For OEM use. End-device certifications such as CE MDR and FDA clearance are held by the customer placing the finished product on the market.

Textus notae sunt tantum referentiae factuales; nullum opus artis accreditationis tertii partis repraesentatur.

OEM/ODM

Conturum cunei, limen, cavi et connexio ad tuum schemam fabricantur.

Privatum label

Tuum nomen commerciale, linguas et opus artis instructionum in facie cunei imprimitur.

MONITORIS CONIUNCTIO

Cunei ad tuum monitorium iam existens vel ad systema vocandi infermorum accommodati sunt.

SAMPLE & PILOT

Exemplaria in 7–12 diebus, productio experimentalis in 20–25 diebus.