Products

SN110

Sterilisation instead of disinfection of instruments in the laboratory. The steriliser complies with all relevant standards and regulations for medical devices.

SN110
Medical Device CE 0197

SN110

Standard delivery Steriliser

The indispensable safety feature for this hot air steriliser: Setpoint Wait. This means that the programme for sterilisation only starts when the set temperature has been reached. This feature can also be used with freely positionable Pt100 temperature sensors. Here the sterilisation time only begins when the set temperature has been reached at all measurement points, and reliable sterilisation is guaranteed at all times.

On this page, you can find all the essential technical data on the Memmert hot air steriliser. Our customer relations team will be pleased to help if you want further information. If you should require a customised special solution, please contact our technical specialists at sales@memmert.com.

Temperature

Setting temperature range +20 to +250 °C
Setting accuracy temperature up to 99.9 °C: 0.1 / from 100 °C: 0.5
Working temperature range at least 5 above ambient temperature to +250 °C
Temperature sensor 1 Pt100 sensor DIN class A in 4-wire-circuit

Control technology

ControlCOCKPIT SingleDISPLAY. Adaptive multifunctional digital PID-microprocessor controller with high-definition TFT-colour display
Timer Digital backwards counter with target time setting, adjustable from 1 minute to 99 days
Function SetpointWAIT the process time does not start until the set temperature is reached
Calibration three freely selectable temperature values
adjustable parameters temperature (Celsius or Fahrenheit), air flap position, programme time, time zones, summertime/wintertime

Ventilation

Convection natural convection
Fresh air Admixture of pre-heated fresh air by electronically adjustable air flap
Vent vent connection with restrictor flap

Communication

Documentation programme stored in case of power failure
Programming AtmoCONTROL software for reading out, managing and organising the data logger via Ethernet interface (temporary trial version can be downloaded). USB stick with AtmoCONTROL software available as accessory (on demand).

Safety

Temperature control adjustable electronic overtemperature monitor and mechanical temperature limiter TB, protection class 1 according to DIN 12880 to switch off the heating approx. 20°C above nominal temperature
Autodiagnostic system for fault analysis

Standard equipment

Works calibration certificate Calibration at +160°C
Door fully insulated stainless steel door with 2-point locking (compression door lock)
Internals 2 stainless steel grid(s), electropolished

Stainless steel interior

Interior easy-to-clean interior,made of stainless steel, reinforced by deep drawn ribbing with integrated and protected large-area heating on four sides
Volume 108 l
Dimensions w(A) x h(B) x d(C): 560 x 480 x 400 mm
Max. number of internals 5
Max. loading of chamber 175 kg
Max. loading per internal 20 kg

Textured stainless steel casing

Dimensions w(D) x h(E) x d(F): 745 x 864 x 584 mm (d +56mm door handle)
Housing rear zinc-plated steel

Electrical data

Voltage Electrical load 230 V, 50/60 Hz
approx. 2800 W
Voltage Electrical load 115 V, 50/60 Hz
approx. 1800 W

Ambient conditions

Set Up The distance between the wall and the rear of the appliance must be at least 15 cm. The clearance from the ceiling must not be less than 20 cm and the side clearance from walls or nearby appliances must not be less than 5 cm.
Altitude of installation max. 2,000 m above sea level
Ambient temperature +5 °C to +40 °C
Humidity rh max. 80 %, non-condensing
Overvoltage category II
Pollution degree 2

Packing/shipping data

Transport information The appliances must be transported upright
Customs tariff number 8419 8998
Country of origin Federal Republic of Germany
WEEE-Reg.-No. DE 66812464
Dimensions approx incl. carton w x h x d: 830 x 1050 x 800 mm
Net weight approx. 74 kg
Gross weight carton approx. 99 kg

Standard units are safety-approved and bear the test marks

CE LGA
VDE
UL

Intended use as medical device

Memmert is bringing medical devices of class I according to EU Directive (EU) 2017/745 into circulation.

Type Intended use as medical device Classification according to (EU) 2017/745
UNmplus, UFmplus The appliance may be used for heating fango, silicate and APS packs for physical therapy and keeping them warm. I
UNm, UFm, INm, IFm The appliance may be used for heating fango, silicate and APS packs for physical therapy and keeping them warm. I
INmplus, IFmplus Im may be used for heating fango, silicate and APS packs for physical therapy and keeping them warm. Implus may be used for temperature control of rinsing and infusion solutions and contrast agents. I
IFbw The appliance is used to heat non-sterile cloths and covers. Any other use is improper
and may cause damage or danger.
I

Memmert is bringing medical devices of class IIa and IIb into circulation according to MDD 93/42/EEC until 31.12.2028 according to the transitional provisions (EU) 2023/607 by the (EU) 2017/745 article 120 (2).

Type Intended use as medical device Classification according to 93/42/EWG
SNplus, SFplus The product is intended for the sterilisation of medical devices with dry heat at atmospheric pressure. IIb
SN, SF The product is intended for the sterilisation of medical devices with dry heat at atmospheric pressure. IIb
ICOmed The CO2 incubator ICOmed is used to generate and maintain constant ambient conditions for the in-vitro fertilisation (IVF) application field, especially for the incubation of oocytes, spermatozoa and zygotes in special culture dishes for IVF application as well as for gene expression and the biosynthesis of RNA and proteins. IIa

Download as pdf

Medical device consultant training

As part of our medical device consultant training, we qualify you in the consultation, use and instruction of our medical products, taking into account the currently applicable legal requirements with regard to the new Medical Devices Regulation (EU) 2017/745. We explain the requirements for dealers, the geographical scope as well as information on the reporting system and the tasks of a medical device consultant. After successful participation, you will receive a certificate of qualification as a medical device consultant for Memmert medical devices.

Have we piqued your interest? Please contact us at sales@memmert.com for more information.