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Miele PG8583 Professional Laboratory Bottle Washer

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Brand Miele
Origin Germany
Model PG8583
Chamber Volume 175 L
Heating Power Not specified (typical for Class B washer-disinfectors)
Wash Temperature Range Adjustable up to 93 °C
Rinse Water Options Deionized water compatible
External Dimensions (L×W×D) 835 × 600 × 600 mm
Cleaning Chemistry ProCare Lab detergent system
Compliance EN ISO 15883-1, EN ISO 15883-4, EN 61000-6-3, EN 61000-6-4
Software Interface Process documentation port (RS232/USB optional
Safety Certification CE-marked as Class B washer-disinfector per EN ISO 15883

Overview

The Miele PG8583 is a Class B laboratory bottle washer–disinfector engineered for high-reproducibility reprocessing of glassware, plasticware, and stainless-steel labware in regulated research, clinical, pharmaceutical, and quality control environments. Based on thermodynamic validation principles and validated thermal disinfection cycles (A0 ≥ 3,000), the PG8583 delivers consistent microbial reduction (≥ log 6 reduction of Geobacillus stearothermophilus spores) through precisely controlled wash, rinse, and thermal disinfection phases. Its 175 L chamber accommodates full-size rack sets—including 1000 mL volumetric flasks, 500 mL centrifuge bottles, Petri dishes, pipette tips, and multi-well plates—while maintaining laminar flow distribution via dual rotating spray arms and pressure-regulated nozzles. Designed and manufactured in Gütersloh, Germany, the unit integrates Miele’s proprietary ProCare Lab chemistry management system, enabling automated dosing, concentration monitoring, and compatibility with low-foaming, residue-free enzymatic and alkaline formulations compliant with ISO 15883-4 Annex A.

Key Features

  • Class B washer–disinfector architecture meeting EN ISO 15883-1 and EN ISO 15883-4 requirements for laboratory reprocessing
  • 175 L stainless-steel chamber with corrosion-resistant 316L lining and integrated condensate recovery system
  • Adjustable thermal disinfection cycle with temperature range from ambient to 93 °C and programmable dwell times (1–30 min)
  • Dual-axis rotating spray arms with 360° coverage and pressure-regulated nozzles ensuring uniform impingement across all load configurations
  • ProCare Lab chemical dosing system with dual-drum capacity (main detergent + neutralizer/rinse aid), auto-calibration, and real-time conductivity-based concentration control
  • Deionized water-compatible final rinse stage with conductivity monitoring (< 1 µS/cm threshold) for trace analysis applications
  • Integrated process documentation interface supporting RS232, USB, or optional Ethernet connectivity for audit-ready data export (CSV/Excel)
  • CE-marked electrical safety compliance (EN 61000-6-3/6-4) and acoustic noise level ≤ 58 dB(A) at 1 m

Sample Compatibility & Compliance

The PG8583 supports standardized reprocessing of common laboratory vessels including borosilicate glass (e.g., Pyrex®, Duran®), polypropylene and polycarbonate consumables, stainless-steel beakers and funnels, and silicone-coated or PTFE-lined components. It is validated for use with ISO 15883-defined load types: Type A (open containers), Type B (partially covered), and Type C (fully sealed). The system conforms to EU Medical Device Regulation (MDR 2017/745) Annex I essential requirements for ancillary equipment used in sterile processing workflows. All standard programs are pre-validated per ISO 15883-4 Annex B protocols and support GLP/GMP documentation requirements—including user access control, electronic signatures (via optional software module), and full audit trail generation per FDA 21 CFR Part 11 when integrated with Miele LabManager software.

Software & Data Management

The PG8583 features an intuitive 7-inch TFT touchscreen HMI with multilingual UI (English, German, French, Spanish, Chinese). Predefined programs include “Trace Analysis,” “Cell Culture,” “Pharma QC,” and “Microbiology,” each with configurable parameters: pre-wash duration, main wash temperature/time, intermediate rinse count, final rinse conductivity threshold, and drying profile. Process logs capture timestamped data for every cycle: inlet water temperature/pressure, detergent dosage volume, chamber temperature curves, rinse conductivity values, and door interlock status. Exported CSV files include ISO-compliant metadata headers for integration into LIMS or ELN platforms. Optional LabManager software enables remote monitoring, centralized fleet management, automated report generation, and electronic signature workflows compliant with 21 CFR Part 11 and EU Annex 11.

Applications

The PG8583 serves critical cleaning needs across multiple regulated domains: trace metal analysis laboratories requiring sub-ppt contamination control; biopharmaceutical QC labs validating container-closure integrity; academic cell culture facilities eliminating endotoxin carryover; clinical microbiology units reprocessing Petri dishes and inoculation loops; and environmental testing labs handling high-volume water sample bottles. Its programmability supports method-specific validation—such as USP for depyrogenation or ASTM E2505-18 for detergent residue assessment—and enables seamless integration into ISO/IEC 17025-accredited quality systems. The unit is routinely deployed in sites undergoing MHRA, FDA, or EMA inspections where documented cleaning efficacy and process traceability are mandatory.

FAQ

Is the PG8583 validated for use in GMP environments?
Yes—the PG8583 is supplied with IQ/OQ documentation templates aligned with ISO 15883-4 and includes built-in tools for performance qualification (PQ) of thermal disinfection cycles.
Can it handle both glass and plastic labware simultaneously?
Yes—its programmable temperature profiles and chemical dosing allow safe co-processing of borosilicate glass, PP, PC, and PS items without warping or leaching.
Does it support deionized water for final rinsing?
Yes—the final rinse stage accepts DI water input with inline conductivity monitoring to ensure < 1 µS/cm residual ion content.
What regulatory standards does it meet?
EN ISO 15883-1/-4 (washer–disinfectors), EN 61000-6-3/-4 (EMC), CE marking per Directive 2014/32/EU (PED), and conformity with Annex I MDR 2017/745 for ancillary equipment.
Is third-party validation support available?
Yes—Miele Professional offers on-site installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) services performed by certified validation engineers.

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