Dual-diode laser.
1470 + 980 nm.

Explore the systems behind S1pro+. Two channels, thermal control and a connection to your practice.

02 / THE CORE OF S1pro+01 — 03
S1pro+ console and control technologyS1pro+ portable formatS1pro+ HD screen and side connection
SIMULTANEOUS DUAL EMISSION

Two wavelengths.
One platform.

1470 nm and 980 nm integrated into one system. A dual architecture to adapt energy to each procedure, according to the protocol and the device’s indications.

1470 nm+980 nm
THERMAL MANAGEMENT

Stability.
From the core.

TEC thermoelectric cooling and independent ventilation channels. A design that manages heat while the system operates.

TEC cooling
STANDARD CONNECTIVITY

Your practice.
More possibilities.

Standard SMA connector for compatible optical fibres. Flexible sourcing, using consumables that meet the manufacturer’s specifications.

SMA standard connector
KEEP EXPLORING
TWO CHANNELS / ONE ARCHITECTURE

Explore the
dual technology.

Two wavelengths integrated into the same platform. Select a channel to explore the diagram.

EMISSION ARCHITECTURE1470 nm + 980 nm
1470 nm 980 nmILLUSTRATIVE DIAGRAM / NOT A CLINICAL SETTING
QUALITY / SAFETY / TRAINING

Technology with supporting documentation.

MANUFACTURERPIOON logo, manufacturer of S1pro+

Regulatory references, technical standards and training: understand what comes with your device.

  • CE 0123European markingModel documentation on request
  • 510(k)Marketing clearanceFDA · K262426
  • ISO13485Medical devicesAs stated by the manufacturer
  • ISO9001Quality managementAs stated by the manufacturer
  • IEC60601-1Electrical safety and essential performanceTesting reported in K262426
  • IEC60825-1Laser safety · Class 4Testing reported in K262426
ACADEMY / INSTITUTO ENDOLÁSER

The 0.01 mm Doctrine

Official Instituto Endoláser certification

The Institute’s own training certification. Separate from the device’s regulatory authorisations.

Explore training

S1Pro+ is listed in FDA 510(k) clearance K262426. Its summary reports IEC 60601-1 and IEC 60825-1 testing. CE and ISO references come from manufacturer information; request the certificates and declaration of conformity for the offered configuration to confirm scope and validity.

Request device documentation
S1 MEDTECH / FOR PROFESSIONALS

The device. The full picture.

S1pro+ is presented as a dual-diode platform for medical professionals. When comparing an endolaser device, identify the model and the configuration quoted, including its emission modes and accessories.

Request the technical data sheet, instructions for use, list of compatible fibres and applicable documentation. The manufacturer’s range may include different versions. Our team can help you gather information about the configuration offered: request S1pro+ documentation.

S1 MEDTECH / LET’S TALK

Your next step, together.

Request information
S1 MEDTECH