The MET ONE HHPC 2+ is a two-channel, 0.5um handheld particle counter designed as an affordable tool for the routine monitoring of controlled environments to ISO 14644 Cleanroom Classifications. Regulated and semi-regulated production environments that adhere to a GMP principle such as aseptically packaged food and beverage filling lines, hospital labs and formulating pharmacies frequently choose the MET ONE HHPC 2+.

Specifications

Platform APC Instruments
Channels/Standard Sizes 2 channels: 0.5 µm plus 1 selected from 1.0, 2.0 OR 5.0 µm
Flow Rate 2.83 L per minute
Zero Count Conforms to JIS B9921 (1 count or less in 5 min; 95% UCL)
Coincidence Loss 10% at 4,000,000/m3 (per ISO-21501-4 method)
Industry Standards 21 CFR Part 11, CE, ISO 14644-1, FCC
Counting Efficiency 50% at 0.5 µm (100% for particles > 0.75 µm)
Count Alarms, Display & Cycles Raw counts: N/CF, N/CM, N/L in cumulative or differential mode, User-defined alarm counts
Data Storage 10,000 records
Interfaces & Protocols USB Client (v1.1), USB Host (v1.1)
Display 3.5" high-resolution (320 x 240) color display
Power Requirements 100-240 VAC, 50/60 Hz, 1.0 A
Temperature Range Operating temperature range: 10°C to 40°C, Storage temperature range: -10°C to 50°C
Environmental Conditions Safe for indoor use only
Humidity Restrictions < 95% non-condensing
Battery Lithium Ion (rechargeable) battery
Battery Operating Time 10+ hours (typical use) / minimum 5.5 hours (continuous sampling)
Battery Recharge Time 3.5 hours
Label Locations Alphanμmeric Location Names
Operating System Windows IE, Safari and Firefox
Color Gray
Weight 0.7 kg / 1.5 lb
Width 27 cm / 10.6 in
Depth 10 cm / 3.9 in
Height 5.3 cm / 2.1 in
Additional Information Concentration limit: 10% at 4,000,000 per ft3 (per ISO 21501) Languages: English, Japanese

NOT ALL PRODUCTS ARE AVAILABLE IN ALL COUNTRIES
PRODUCT AVAILABILITY AND REGULATORY STATUS DEPENDS ON COUNTRY REGISTRATION PER APPLICABLE REGULATIONS

The listed regulatory status for products correspond to one of the below:
IVD: In Vitro Diagnostic Products. These products are labeled "For In Vitro Diagnostic Use."
ASR: Analyte Specific Reagents. These reagents are labeled "Analyte Specific Reagents. Analytical and performance characteristics are not established."
CE: Products intended for in vitro diagnostic use and conforming to European Directive (98/79/EC). (Note: Devices may be CE marked to other directives than (98/79/EC)
RUO: Research Use Only. These products are labeled "For Research Use Only. Not for use in diagnostic procedures."
LUO: Laboratory Use Only. These products are labeled "For Laboratory Use Only."
No Regulatory Status: Non-Medical Device or non-regulated articles. Not for use in diagnostic or therapeutic procedures.