OverviewCombined fridge‑freezer certified as a medical device for storage of blood and plasma in two independent compartments within a single unit with two glass doors and dual cooling systems. The PLASMA‑VISION 2T 500 TOUCH stores blood at positive temperatures and plasma at negative temperatures simultaneously. Integrated 7" touch controller with graphical logging and independent DMLP TOUCH board with backup battery for data recording and alarms during power failure. Device compliant with Directive 93/42/EEC (class IIa) and amendment 2007/47/EEC; registered in the MD Repertoire of the Italian Ministry of Health. RoHS 2011/65/CE compliant.
Key data- Temperature ranges: +2/+6 °C (blood) | -10/-20 °C (plasma)
- Gross capacity: 486 L (17.16 cu ft)
- External dimensions (WxDxH): 72 x 76 x 208 cm
- Controller: TOUCH (7" full touch screen)
Structure and refrigeration- Inner dimensions (each compartment): 60 x 58.8 x 70 / 60 x 58.8 x 74 cm
- Nominal capacity: 250 + 250 L; Net capacity: 249 + 230 L
- Insulation: injected PUF, 43 kg/m3, water‑based injection, CFC‑free; thickness 75 mm (back) / 60 mm (sides)
- Structure: monocoque construction in white plastified steel with antibacterial film; rounded inner corners; 4 unidirectional rollers and 2 front feet
- Interior lighting: full‑height LED, dimmable
- Refrigeration: professional ventilated; adaptive automatic defrost with condensate evaporation; Night & Day energy reduction
Controller- 7" full touch microprocessor controller — resolution 0.1 °C, accuracy ±0.3 °C
- Temperature and alarm recording, multi‑trace real‑time graph, current temperature and editable setpoint, editable alarm limits, energy consumption and battery status
- Slots/ports: 3 SD card slots (data history), USB port (download/update), SIM slot for optional GSM module
- Connectivity: integrated web server for LAN (RJ45) and MODBUS TCP/IP; dry contact for remote alarm
- Safety: anti‑freeze and anti‑overheat devices; acoustic and visual alarms (muting available) recorded with date/time/type/duration/peak temperature
- DMLP TOUCH module: independent temperature and alarm recording with backup battery (records during power failure); product temperature simulation probe; external terminal board for dry contact and RJ45
- Upgradeable with GSM and Wi‑Fi; compatible with local or cloud monitoring systems; electric digital lock optional
Technical data- Refrigerant: R290
- Energy consumption: 5.5 kWh/24h
- Power absorption / current: kW 0.17 + 0.32 / Amp 1 + 2.3
- Inrush current: Amp 3 + 5
- Noise level: <50 dBA
- Heat rejection EN 12900: W 229
- Shelves included: 4 (2+2); max shelves: 3+3; wire shelf size: 56 x 55 cm
- Drawers max: 5+3; drawers with dividers (each compartment): 15 x 50 x 7.5 cm (3); drawers without dividers: 49 x 50 x 7.5 cm
Accessories / options- Gateway IOT
- Local monitoring system FIOCCHETTI LAN SUPERVISOR
- GSM module
- Wi‑Fi module
- 4‑20mA converter module
- Shelf for model 500
- Pull‑out aluminum drawer with dividers for model 500
- Pull‑out aluminum drawer without dividers for model 500
- Lockable drawer for narcotics
- Plexiglass front for drawers
- Access port Ø 35 mm with stopper
- Stainless steel wire racks (various sizes)
- Wheels kit (2 with brakes) for model 500
- Port hole Ø 15 mm
- Humidity probe
- PT100 probe (free contacts)
- Power supply options: 220V/1~/60Hz or 115V/1~/60Hz
- Voltage stabiliser
- Wooden crate packaging
Product specifications- Product name / model: PLASMA‑VISION 2T 500 TOUCH
- Code: DMD0502
- Series: PLASMA‑VISION 2T
- Function: combined refrigerator + freezer for blood and plasma with two glass doors and double cooling unit
- Temperature ranges: +2/+6 °C (blood) and -10/-20 °C (plasma)
- Gross capacity: 486 L; External dimensions (WxDxH): 72 x 76 x 208 cm
- Insulation: PUF 43 kg/m3, CFC‑free, water‑based injection
- Controller: 7" full touch screen with data logging, SD/USB, RJ45, DMLP TOUCH with backup battery
- Alarms & recording: visual and acoustic alarms; event logging with date/time/type/duration/peak temperature
- Compliance: Directive 93/42/EEC (class IIa) and amendment 2007/47/EEC; registered in Italian Ministry of Health MD Repertoire; RoHS 2011/65/CE