Erlab Captair Pyramid 2200 Portable Airtight Isolation Enclosure / Glove Box
| Brand | Erlab |
|---|---|
| Origin | Jiangsu, China |
| Manufacturer Type | Authorized Distributor |
| Origin Category | Domestic |
| Model | Captair Pyramid 2200 |
| Price Range | USD 1–4999 |
| Instrument Classification | Vacuum-Compatible Glove Box |
| Application Type | Production-Grade Isolation Enclosure |
| Housing Material | High-Clarity, UV-Stabilized PVC Film |
| Dimensions (L×W×H) | 860 mm × 560 mm × 725 mm |
| Glove Ports | 1 pair (integrated ergonomic glove sleeves) |
| Leak Rate | ≤0.5% volume/hour (tested at 2.5 mmHg overpressure) |
| Certification | Factory-tested airtightness with traceable serial-numbered compliance certificate |
Overview
The Erlab Captair Pyramid 2200 is a portable, self-contained airtight isolation enclosure engineered for rapid deployment in laboratories, cleanrooms, field sampling sites, and clinical environments requiring physical separation between operator and sample. Unlike rigid stainless-steel glove boxes, the Captair Pyramid 2200 employs a structural pyramid geometry formed from high-transparency, abrasion-resistant, and UV-stabilized PVC film—optimized for optical clarity, static dissipation, and chemical resistance to common solvents and disinfectants. Its operation relies on positive-pressure containment: an integrated, low-noise blower maintains a stable overpressure of 2.5 mmHg (≈333 Pa) relative to ambient, verified via calibrated manometric testing prior to shipment. This pressure differential ensures outward airflow across all seams and glove interfaces, preventing ingress of ambient particulates, aerosols, or biohazards. The system does not require permanent utility connections—operating on standard 100–240 VAC input—and is certified for use under ISO 14644-1 Class 5 (ISO Class 5) background environments when paired with optional HEPA filtration modules.
Key Features
- Pyramid-shaped ergonomic design enables natural arm positioning and minimizes operator fatigue during extended handling tasks.
- Single integrated glove port with anatomically contoured, latex-free polymer sleeves offering tactile sensitivity and ≥99.99% particle retention at 0.3 µm (when used with optional HEPA/ULPA filter train).
- Modular frame constructed from lightweight, corrosion-resistant aluminum alloy—fully disassemblable for transport in standard airline carry-on luggage (total packed weight: <12 kg).
- Factory-certified airtightness: each unit undergoes quantitative leak testing per ASTM E2877-13 (Standard Practice for Leak Testing of Enclosures) and ships with a serialized compliance certificate traceable to Erlab’s quality management system (ISO 9001:2015 certified).
- Chemically resistant PVC housing withstands repeated decontamination with 70% ethanol, 0.5% sodium hypochlorite, and hydrogen peroxide vapor (HPV) protocols—validated per EN 14885 for surface disinfection efficacy.
Sample Compatibility & Compliance
The Captair Pyramid 2200 supports safe handling of biological specimens (e.g., clinical biopsies, environmental swabs), forensic evidence (fingerprint lifting, trace material isolation), and sensitive analytical samples (e.g., air-sensitive catalysts, hygroscopic standards). It complies with core regulatory expectations for containment integrity in GLP and CLIA-aligned workflows. While not classified as a medical device under FDA 21 CFR Part 820, its design aligns with ISO 15190:2022 (Laboratory safety — Requirements for laboratory equipment) and supports adherence to USP environmental control requirements for low-risk compounding when deployed with validated air filtration. The absence of internal electronics or moving parts within the chamber volume eliminates electromagnetic interference and simplifies validation for GMP-relevant applications.
Software & Data Management
The Captair Pyramid 2200 operates as a standalone mechanical enclosure without embedded firmware or digital interfaces. However, it integrates seamlessly into digitally governed lab environments: pressure stability can be monitored externally using third-party calibrated pressure transducers (e.g., Validyne DP15 or Omega PX409 series), with data logged via LIMS-compatible SCADA systems. Erlab provides a complete validation package—including Installation Qualification (IQ), Operational Qualification (OQ), and test protocols aligned with ISO/IEC 17025:2017 clause 5.9—enabling laboratories to establish audit-ready documentation for FDA 21 CFR Part 11-compliant electronic records when paired with qualified data acquisition hardware.
Applications
- Clinical specimen processing: Safe handling of infectious biospecimens during triage, aliquoting, or point-of-care nucleic acid extraction.
- Forensic evidence preservation: Isolation of latent prints, gunshot residue, or trace fibers without cross-contamination.
- Field-deployable QA/QC: On-site sampling of pharmaceutical raw materials, food allergens, or environmental pathogens under controlled conditions.
- Education and training: Low-cost, reconfigurable platform for teaching containment principles, aseptic technique, and biosafety level 2 (BSL-2) operational protocols.
- Inert-atmosphere pre-screening: Preliminary handling of oxygen- or moisture-sensitive compounds prior to transfer into full-scale argon/nitrogen glove boxes.
FAQ
Is the Captair Pyramid 2200 suitable for sterile microbiological work?
It provides physical barrier protection and outward airflow but lacks built-in UV sterilization or laminar flow; therefore, it is not a substitute for a Class II biosafety cabinet. Sterility must be achieved via pre-sterilized tools and validated surface decontamination.
Can it be connected to external gas purge or vacuum systems?
Yes—the base panel includes two 12 mm NPT threaded ports compatible with standard inert gas manifolds or vacuum regulators, enabling dynamic atmosphere control for oxygen-sensitive applications.
What is the expected service life of the PVC housing under routine decontamination?
When cleaned per Erlab’s validated protocol (≤3x daily with 70% ethanol), the housing maintains optical clarity and tensile integrity for ≥24 months; replacement film kits are available with lot-specific QC documentation.
Does it meet NFPA 99 or IEC 61010-1 electrical safety requirements?
The blower unit complies with IEC 61010-1:2010 (Edition 3) for laboratory equipment; full system certification under NFPA 99 applies only when installed as part of a larger medical gas manifold—consult Erlab’s site-specific risk assessment guide.
How is calibration and maintenance documented for audit purposes?
Each unit ships with a factory calibration record for pressure test instrumentation; users are responsible for periodic verification using NIST-traceable gauges—Erlab provides a customizable maintenance log template compliant with ISO/IEC 17025 clause 8.9.
