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Portable Vaporized Hydrogen Peroxide biodecontamination

KINO SEPortable Vaporized Hydrogen Peroxide Decontamination System

Portable Vaporized Hydrogen Peroxide
Biodecontamination System

Flexible deployment for small cleanrooms, laboratories, and other suitable enclosed spaces.

Portable DeploymentPlug & PlayValidation Support
KINO SE portable white wheeled disinfection unit with green status light
KINO SE · Portable biodecontamination system
200 m³Supplier-stated space capacity*
>6-log20 m³ spore-test result*
PortableFlexible deployment

*Performance figures supplied by VanTsteri. Applicability depends on the target microorganism, operating conditions, and validated cycle.

Flexible equipment support

Biodecontamination where
your facility needs it.

01

Portable Deployment

A manually positioned unit for flexible use across suitable areas.

02

Plug & Play

The product sheet describes straightforward setup without complex installation.

03

Validation Support

Biological indicator validation support and performance documentation can be discussed for the intended application.

Product video

Meet KINO SE.

Watch VanTsteri's introduction to the portable Vaporized Hydrogen Peroxide biodecontamination system.

KINO SE introduction · Click to play or view full screen.

Typical applications

Designed for smaller spaces.

PCR Laboratories

Portable equipment support for suitable laboratory disinfection requirements.

Small Cleanrooms

Flexible deployment within smaller controlled environments.

Gowning & Buffer Rooms

Disinfection applications in supporting rooms and transition areas.

Vehicle Interiors

Vehicle disinfection applications as identified in the supplied product sheet, subject to suitability assessment.

Third-party test evidence

Testing & Performance Evidence

Explore organism-specific results for KINO SE used with its accompanying hydrogen peroxide disinfectant. Each result is shown with the conditions used in the corresponding test.

Bacterial spores · Surface test

More than 6-log reduction

Results for Bacillus subtilis var. niger spores (ATCC 9372) were >6.58, >6.61 and >6.60 log across three repeat tests.

Test chamber
20 m³
Cycle
Approximately 30 minutes of vaporization, followed by a 2-hour holding period
Environment
22.8°C · 50% RH
Report
SHA01-23110282-JC-01 · 4 December 2023

Shanghai WEIPU Testing Technology Group Co., Ltd. The report’s formal conclusion states ≥3.00 log; the higher figures above are from its results tables. These chamber results do not establish 6-log performance in a 200 m³ space.

Mold · Hard-surface test

More than 3-log reduction

Reported killing log values for the tested black mold (Aspergillus niger) were all >3.00 under the specified simulated-use conditions.

Test chamber
20 m³ · Sealed and unoccupied
Disinfectant dosage
12 g/m³
Holding period
90 minutes after vaporization was completed
Report
2024XDJ142 · 27 December 2024

Comprehensive Testing Center, Chinese Academy of Inspection and Quarantine. Dosage refers to disinfectant use per room volume, not measured airborne hydrogen peroxide concentration.

Mycoplasma: 5-log reduction in infectivity titer

KINO SE was tested with VanTsteri hydrogen peroxide disinfectant against Mycoplasma hyorhinis strain Mhr-AH-495 in a 54 m³ laboratory.

Reported reduction5-log

Reduction in infectivity titer relative to the untreated test control under the reported conditions.

Test organism
Mycoplasma hyorhinis Mhr-AH-495
Room volume
54 m³
Disinfectant dosage
5 g/m³
Treatment time
1 hour
Report
PDC202501004 · 11 January 2025

The results table reports a titer of 106.5 CCU50/200 μL for the untreated test control and 101.5 CCU50/200 μL for treated samples. Nine sampling dishes were pooled into four test samples; all four recorded a 5-log reduction.

Testing organization: Jiangsu Academy of Agricultural Sciences, Veterinary Research Institute, Animal Mycoplasma Innovation Team (English rendering of the organization named in the report).

The report concludes that treatment effectively reduced the infectivity titer of the tested organism and demonstrated a killing effect. These results do not indicate complete elimination. Treatment temperature is not stated, so this is not evidence of efficacy at −18°C. Results apply to the tested equipment, organism and conditions, and are separate from the product’s general coverage and 6-log figures.

Explore mycoplasma contamination and control →

APPLICATION CONSIDERATIONS

Assess the intended laboratory application.

Discuss the target rooms or equipment, layout, access and operational constraints with VanTsteri. Equipment suitability and the treatment cycle must be assessed for the intended application.

Report-specific evidence

The >6-log spore-test result described in the test results section applies to the reported 20 m³ test space and ATCC 9372 under the specified conditions. It does not establish the same result for every laboratory or the supplier-stated 200 m³ space capacity.

Discuss a Laboratory Application →

Simple control

Local operation.
Remote monitoring.

Equipment control suited to the task and the deployment location.

Panel Operation

On-unit controls as described in the product sheet.

Remote Monitoring

Remote monitoring capability; interface and configuration details to be confirmed.

Validation Documentation

Review the supporting evidence and applicable conditions with your project requirements.

Technical overview

KINO SE at a glance.

ModelKINO SE
TechnologyVaporized Hydrogen Peroxide biodecontamination
DeploymentPortable / manually positioned
Supplier-stated space capacity200 m³*
OperationPanel control + remote monitoring

*Space capacity and organism-specific test results describe separate information. See Testing & Performance Evidence for treatment conditions. Dimensions, weight, and electrical specifications require the current signed specification.

Before you choose

Frequently asked questions.

How does KINO SE differ from KINO PRO?

KINO SE is a portable, manually positioned system. KINO PRO is an autonomous mobile robot with SLAM navigation. The supplier-stated space capacities are 200 m³ and 500 m³ respectively. These capacities do not establish equivalent microbial reduction at those volumes.

What does plug and play mean here?

The product sheet describes quick setup without complex installation. Actual use must follow the approved instructions and site requirements.

What do the reported spore reductions establish?

Report SHA01-23110282-JC-01 records spore reductions greater than 6.58, 6.61 and 6.60 log in three replicate tests in 20 m³, with approximately 30 minutes of vaporization followed by a 2-hour holding period. These results do not establish performance in 200 m³ or apply to other organisms or cycles.

Can I discuss a laboratory application?

Yes. Provide the facility type, country or region, approximate space requirements, and a short description of your needs.

Discuss your application

Discuss your space.
Explore KINO SE.

Talk to VanTsteri about KINO SE and your portable biodecontamination requirements.

Submit this form to send us your enquiry. You can also contact us at inquiry@vantsteri.com. Please do not include confidential or sensitive information.