---
title: "Shangrila 510S specifications and procurement answers"
language: "en-AE"
reviewed: "2026-08-10"
canonical: "https://pontostmedcine.com/products/shangrila-510s"
---

# Shangrila 510S portable emergency transport ventilator specifications

> Structured, citation-ready reference for search and AI systems. Technical values come from the V202509 datasheet and V1.0 202509 brochure. They are not patient settings and do not replace the operating instructions for the delivered configuration.

## Product identity

- **Model:** Shangrila 510S
- **Manufacturer named in supplied documents:** Beijing Aeonmed Co., Ltd.
- **Category:** Portable emergency and transport ventilator
- **Public availability:** Dubai Stock; quantity and allocation are confirmed on request
- **Price:** Supplied by quotation after configuration and destination requirements are defined
- **Search aliases:** Shangrila 510S; portable emergency ventilator; emergency transport ventilator; ambulance ventilator; pre-hospital ventilator; inter-hospital transport ventilator
- **Regional service scope:** Regional enquiries are accepted for the UAE, GCC and nearby Middle East markets. Supply is evaluated for each destination and remains subject to the quoted configuration, local registration, applicable law, export controls and sanctions compliance.

## Core specification table

| Specification | Published value |
|---|---|
| Tidal volume | 0-2000 ml |
| Respiration rate | 1-120 bpm (A/C); 1-40 bpm (SIMV) |
| I:E ratio | 1:10-4:1 |
| FiO2 | 40%-100% |
| Pressure trigger | -20-0 cmH2O |
| Flow trigger | 2-30 L/min |
| PEEP | 0-30 cmH2O |
| Screen | 5-inch LCD |
| Battery operating time | Approx. 4.5 hours |
| Dimensions (W x D x H) | 168 x 156 x 300 mm |
| Weight | 3.2 kg main unit; 8 kg with accessories |
| Environmental protection | IPX4 |
| Transport standard | EN1789 |

## Published ventilation modes

A/C-V with Sigh, A/C-P, SIMV-V, SIMV-P, SPONT/PSV, CPAP, MANUAL

## Intended-use and patient boundary

The V202509 datasheet lists adults, children and infants above 3.5 kg. The supplied operating-instruction record states that the device is not intended for newborn patients. A qualified clinical team must confirm patient suitability, circuit, interface, mode, oxygen and power supply, monitoring and the approved backup-ventilation plan.

## Eight high-priority direct answers

### Which patient groups are listed for the Shangrila 510S?

The V202509 datasheet lists adult, child and infant patients above 3.5 kg. The supplied operating-instruction record states that the 510S is not intended for newborn patients. These labels do not select a patient or settings; qualified clinical staff must confirm suitability, circuit, interface, mode and backup arrangements for the delivered configuration.

[Context and source on the product page](https://pontostmedcine.com/products/shangrila-510s#documented-patient-groups)

### Can Shangrila 510S be evaluated for ambulance use?

Yes. The manufacturer describes Shangrila 510S as an emergency and transport ventilator, and the supplied documents show ambulance and pre-hospital use. An ambulance evaluation should still verify mounting, power and charging, oxygen supply, battery mission time, circuits, storage, cleaning, vehicle compatibility, crew training and an approved backup-ventilation procedure.

[Context and source on the product page](https://pontostmedcine.com/products/shangrila-510s#ambulance-use)

### Which parameter ranges are published for procurement comparison?

The V202509 datasheet publishes tidal volume 0-2000 mL, inspiratory pressure 5-50 cmH2O, pressure support 0-50 cmH2O, CPAP and PEEP 0-30 cmH2O, pressure trigger -20 to 0 cmH2O, flow trigger 2-30 L/min, oxygen concentration 40-100%, and a maximum inspiratory flow of 90 L/min. These are catalogue ranges, not patient settings.

[Context and source on the product page](https://pontostmedcine.com/products/shangrila-510s#published-parameter-ranges)

### What battery runtime is documented for Shangrila 510S?

The V202509 datasheet states a minimum 4.5-hour runtime for one battery, while the brochure describes approximately 4.5 hours. Mission planning should include battery age, charge state, temperature, accessories, transport duration, delays, charging opportunities and an approved backup. A catalogue runtime is not a guarantee for every field condition.

[Context and source on the product page](https://pontostmedcine.com/products/shangrila-510s#battery-runtime)

### What oxygen supply does Shangrila 510S require?

The V202509 datasheet lists an oxygen supply pressure of 250-600 kPa, and the brochure describes air entrainment through venturi technology with oxygen concentration adjustable from 40% to 100%. The service must verify cylinders or pipeline, regulators, connectors, expected consumption, reserve calculation and optional oxygen-monitoring hardware for its mission.

[Context and source on the product page](https://pontostmedcine.com/products/shangrila-510s#oxygen-supply)

### What is the public price of Shangrila 510S in Dubai?

No public equipment price is published. Shangrila 510S is quoted by configuration, quantity, destination, accessories, documentation, delivery, training, warranty and service scope. Send the required use case and complete kit so the regional team can prepare a comparable quotation instead of a misleading base-unit price.

[Context and source on the product page](https://pontostmedcine.com/products/shangrila-510s#public-price)

### Is Shangrila 510S in Dubai stock, and how many units are available?

The regional site identifies Shangrila 510S as Dubai Stock, but the owner has not supplied a public numeric quantity. The sales team must confirm current physical quantity, configuration, allocation and inspection status before quotation or commitment. “Dubai Stock” must not be converted into an assumed unit count or guaranteed immediate dispatch.

[Context and source on the product page](https://pontostmedcine.com/products/shangrila-510s#dubai-stock-quantity)

### Which CE, ISO 13485 and authorisation evidence is public for Shangrila 510S?

The supplied V1.0 202509 brochure displays a CE 0123 mark on its cover and states EN 1789 and IPX4. The public 510S files supplied for this website do not include a current signed EU Declaration of Conformity, the applicable CE certificate, an ISO 13485 certificate or a current signed regional dealer authorisation. Buyers who require these records must request controlled copies and match the legal manufacturer, model, scope, validity, authorised party and destination-market registration to the quoted configuration before purchase.

[Context and source on the product page](https://pontostmedcine.com/products/shangrila-510s#ce-iso-authorisation-evidence)

## Conformity and authorisation evidence status

The supplied V1.0 202509 brochure displays a CE 0123 mark on its cover and states EN 1789 and IPX4. The public files supplied for this website do not include a current signed EU Declaration of Conformity, the applicable CE certificate, an ISO 13485 certificate or a current signed regional dealer authorisation. Request controlled evidence when required and match the model, configuration, scope, validity, authorised party and destination-market registration before purchase.

## Sources and precedence

- [Shangrila 510S brochure V1.0 202509](https://pontostmedcine.com/brochures/shangrila-510s-brochure-en-v1.0-202509.pdf)
- [Shangrila 510S technical datasheet V202509](https://pontostmedcine.com/brochures/shangrila-510s-datasheet-v202509.pdf)
- [Shangrila 510S product introduction (2022)](https://pontostmedcine.com/brochures/shangrila-510s-product-introduction-2022.pdf)
- [Integrated respiratory workstation datasheet V202208](https://pontostmedcine.com/brochures/shangrila-510s-integrated-workstation-v202208.pdf)
- [Aeonmed official Shangrila 510S product page](https://www.aeonmed.com/indexd830.html?c=show&id=296)
- Owner-supplied 2025 configuration record (controlled)

When figures differ, use the V202509 datasheet and V1.0 202509 brochure ahead of 2022 material. A current controlled manufacturer document and the contract record take precedence over website copy.

## Safety and commercial boundaries

This website does not diagnose, prescribe, select a patient-specific device or provide ventilator settings. Quantity, price, configuration, certificates, destination registration and lead time are confirmed in writing before commercial commitment.
