It is our hard-lined commitment to quality that has made Memmert a reliable partner in the medical sector and medical research industry ever since the company’s founding in 1947. Of course we are DIN EN ISO 13485 certified since many years. The following products are classified as medical device. Memmert is bringing medical devices of class I according to the regulation MDR (EU) 2017/745 into circulation. Memmert is bringing medical devices of class IIa and IIb into circulation according to MDD 93/42/EEC until 26 May 2024 according to the transitional provisions by the (EU) 2017/745 article 120 (2).
ICO105med
Standard delivery CO2 incubator ICOmed
On this page, you can find all the essential technical data on the Memmert CO2 incubator ICOmed. 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
| Working-temperature range |
5 °C above ambient temperature up to +50 °C
Standard sterilisation programme: 60 minutes at 180°C (without removing the sensors) |
| Setting temperature range |
+18 to +50 °C |
| Setting accuracy temperature |
0.1 °C |
| Temperature sensor |
2 Pt100 sensors DIN Class A in 4-wire-circuit for mutual monitoring, taking over functions in case of an error |
| Temperature variation in chamber |
at + 37 °C +/- 0.3 K |
| Temperature fluctuations with time |
at 37 °C +/- 0.1 K |
Humidity
| Humidity control (standard) |
Humidity limitation thanks to a Peltier element; when water dish is full and inserted, the Peltier element limits the value of relative humidity in the interior to 93 % rh +/- 2.5 % |
| Setting accuracy humidity |
0.5 % rh |
| Setting range active humidity control (with option K7) |
40 to 97 % rh and rh-Off |
Control of standard components
| CO2 control |
Digital electronic CO2 control with dual beam NDIR system, with auto-diagnostic system and acoustic fault indication, barometric pressure compensation |
| Adjustment range CO2 |
0 to 20 % CO2 |
| Setting accuracy CO2 |
0,1% |
| Variation in time CO2 |
+/- 0.2 % CO2 |
| Adjustment range O2 |
1 to 20 % O2 |
| Setting accuracy O2 |
0.1 % O2 |
Control technology
| ControlCOCKPIT |
TwinDISPLAY. Adaptive multifunctional digital PID-microprocessor controller with 2 high-definition TFT-colour displays. |
| Language setting |
German, English, Spanish, French, Polish, Czech, Hungarian |
| Function SetpointWAIT |
the process time does not start until the set temperature is reached |
| Adjustable parameters |
temperature (Celsius or Fahrenheit), CO2, programme time, time zones, summertime/wintertime |
Communication
| Interface |
Ethernet LAN, USB |
| Documentation |
programme stored in case of power failure |
| Programming |
AtmoCONTROL software on a USB stick for programming, managing and transferring programmes via Ethernet interface or USB port |
Safety
| AutoSAFETY |
additionally integrated over- and undertemperature protection "ASF", automatically following the setpoint value at a preset tolerance range, alarm in case of over- or undertemperature, heating function is switched off in case of overtemperature, cooling function in case of undertemperature |
| Autodiagnostic system |
integral fault diagnostics for temperature and CO2 |
| Alarm |
visual and acoustic |
Heating concept
| 6 sides |
large-area multi-function heating system on four sides with additional door and back heating to avoid condensation |
Standard equipment
| Works calibation certificate |
Works calibration certificate at +37 °C, 5 % CO2 and 90 % rh (requires option K7); standard equipment for units with active humidity control |
| Works calibation certificate |
Works calibration certificate at +37 °C, 5 % CO2, 90 % rh and 10 % O2 (requires option K7 and option T6); standard equipment for units with O2 control |
| Works calibation certificate |
incl. works calibration certificate (measuring point chamber centre) at +37°C, 5 % CO2 for standard units |
| Door |
fully insulated stainless steel door with 2-point locking (compression door lock) |
| Door |
inner glass door with opening (8 mm Ø) to take gas sample |
| Standard equipment |
CO2 connection set: hose with coupling and clamp |
| Standard accessories |
Membrane filter (in order to remove impurities and pollutants, all incoming gases pass through a membrane filter before they reach the chamber) |
| Internals |
2 perforated stainless steel shelf/shelves |
| Internals |
1 stainless steel water dish |
Stainless steel interior
| Dimensions |
w(A) x h(B) x d(C): 560 x 480 x 400 mm (d less 35 mm for fan) |
| Interior |
material 1.4301 (ASTM 304), corrosion resistant |
| Volume |
107 l |
| Max. number of internals |
6 |
| Max. loading of chamber |
90 kg |
| Max. loading per internal |
15 kg |
Textured stainless steel casing
| Dimensions |
w(D) x h(E) x d(F): 719 x 850 x 591 mm (d +56mm door handle) |
| Housing |
rear zinc-plated steel |
Electrical data
| Voltage
Electrical load |
230 V, 50/60 Hz
approx. 1300 W |
| Voltage
Electrical load |
115 V, 50/60 Hz
approx. 1300 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. |
| Ambient temperature |
10 °C to 35 °C |
| Humidity rh |
max. 70 %, non-condensing |
| Altitude of installation |
max. 2,000 m above sea level |
| 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: 800 x 1030 x 800 mm |
| Net weight |
approx. 75 kg |
| Gross weight carton |
approx. 100 kg |
Standard units are safety-approved and bear the test marks
Intended use as medical device
Memmert is bringing medical devices of class I according to EU Directive 93/42/EEC into circulation until the regulation MDR (EU) 2017/745 comes into force. After the new regulation comes into force, Memmert will bring medical devices of class I into circulation according to MDR.
| Type |
Intended use as medical device |
Classification according to MDD |
| 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 |
The appliance may be used for temperature control of rinsing and infusion solutions and contrast agents. |
I |
| IFbw |
The appliance may be used for heating non-sterile covers and cloths. |
I |
Memmert is bringing medical devices of class IIa and IIb into circulation according to MDD 93/42/EEC until 26 May 2024 according to the transitional provisions by the (EU) 2017/745 article 120 (2).
| Type |
Intended use as medical device |
Classification according to MDD |
| 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 appliance is intended for the creation and maintenance of constant environmental conditions for application in the field of in vitro fertilisation (IVF), 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
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.
