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RWD R630 Dual-Canister Veterinary Anesthesia Machine

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Brand RWD
Origin Guangdong, China
Manufacturer Type Direct Manufacturer
Country of Origin China
Model R630
Price Upon Request
Vaporizer Calibration Method Laser Calibration
Isoflurane Output Range 0.50–5.00%
Sevoflurane Output Range 0.50–8.00%
Output Accuracy ±0.10% (0–1%), ±0.15% (>1%)
Anesthetic Capacity per Canister 120 mL (between min/max fill lines)
Operating Temperature 10–35 °C
Gas Flow Range 0.2–10 L/min
Relative Humidity Range 5–90% RH
Dimensions (H×D×W) 206 × 210 × 140 mm
Weight 3.85 kg
Flowmeter Options 0–1 L/min or 0–4 L/min
CO₂ Absorber Volume 2.1 L
Scrubber Canister Net Weight 800 g
Effective Absorbent Increment 200 g
Scrubber Weighing Alarm Threshold >1000 g (for R510-31 canister)
Weighing Resolution 1 g
Rebreathing Circuit Low-resistance, coaxial, semi-closed type
Non-rebreathing Circuit Mapleson F (Magill-type)
Breathing Bag Volumes 0.5 L, 1 L, 2 L
Compatible Species Dogs, cats, pigs, non-human primates, avian and reptilian species (≤50 kg body weight)

Overview

The RWD R630 Dual-Canister Veterinary Anesthesia Machine is an engineered solution for precision-controlled inhalational anesthesia in preclinical research and veterinary clinical settings. Designed around a dual-vaporizer architecture with independent, zero-cross-contamination pathways, the R630 enables rapid, safe switching between isoflurane and sevoflurane without manual vaporizer removal or system purging—eliminating inter-agent carryover and supporting protocol flexibility across diverse animal models. Its core delivery principle relies on calibrated variable-bypass vaporization, where carrier gas flow is split between a temperature-compensated bypass channel and a heated, precisely metered anesthetic-saturated chamber. Laser-based calibration ensures long-term stability of concentration output, critical for longitudinal studies requiring high inter-session reproducibility. The system operates within a defined physiological gas flow range (0.2–10 L/min), accommodating both low-flow rebreathing and high-flow non-rebreathing modes, and meets fundamental safety requirements for veterinary use including fail-safe oxygen monitoring, pressure relief valves, and visual/audible alarm integration.

Key Features

  • Dual independent vaporizers with patented zero-serial-contamination design—enables seamless, immediate transition between isoflurane and sevoflurane
  • Laser-calibrated vaporizer output with documented accuracy: ±0.10% (0–1% range) and ±0.15% (>1% range)
  • Integrated low-resistance coaxial semi-closed rebreathing circuit (1.5 m length) and optional Mapleson F non-rebreathing configuration
  • Modular flowmeter selection: user-selectable 0–1 L/min or 0–4 L/min ranges for precise low-flow applications
  • 2.1 L CO2 absorber capacity with standardized R510-31 scrubber canister interface and digital weighing support (1 g resolution, >1000 g alarm threshold)
  • Compact footprint (206 × 210 × 140 mm) and lightweight chassis (3.85 kg) suitable for mobile cage-mount, benchtop, or trolley-based deployment
  • Environmental operating envelope: 10–35 °C ambient temperature, 5–90% RH—validated for stable performance across standard vivarium conditions

Sample Compatibility & Compliance

The R630 supports safe, titratable anesthesia delivery across a broad spectrum of laboratory and companion animals, including dogs, cats, swine, non-human primates, avian species, and reptiles—with validated efficacy up to 50 kg body weight. Its dual-canister architecture accommodates species-specific agent preferences (e.g., sevoflurane for rapid induction in birds; isoflurane for stable maintenance in rodents and larger mammals). While not FDA-cleared for human use, the device conforms to IEC 60601-1 (general safety) and IEC 60601-2-13 (particular requirements for anesthetic equipment) principles in mechanical and electrical design. All gas pathway materials comply with USP Class VI biocompatibility standards. The system supports GLP-compliant documentation workflows through external data logging interfaces and provides traceable vaporizer calibration records aligned with ISO/IEC 17025 laboratory quality management expectations.

Software & Data Management

The R630 operates as a hardware-integrated analog control platform—no embedded firmware or touchscreen UI. All operational parameters are manually set via calibrated dials and verified visually on analog flowmeters and concentration scales. This design prioritizes reliability, electromagnetic immunity, and audit readiness in regulated environments. For integration into electronic lab notebooks (ELN) or facility-wide anesthesia monitoring networks, analog output signals (e.g., O2 pressure, flow rate) may be interfaced via optional 4–20 mA transducers. Calibration logs—including laser verification timestamps, vaporizer serial numbers, and technician signatures—are maintained externally per institutional SOPs. The absence of proprietary software eliminates cybersecurity vulnerabilities and simplifies 21 CFR Part 11 compliance when paired with validated third-party data acquisition systems.

Applications

  • Longitudinal neuroimaging studies in non-human primates requiring repeated, stable anesthetic depth over multiple sessions
  • Surgical preparation and maintenance in canine and porcine translational models, particularly where rapid recovery and minimal metabolic interference are essential
  • Avian and reptilian anesthesia protocols where rapid agent washout and precise low-concentration control (<1% sevoflurane) are physiologically critical
  • Teaching laboratories conducting comparative pharmacokinetic demonstrations across volatile agents
  • Vivarium satellite stations supporting multi-cage anesthesia workflows with shared O2 supply and centralized gas distribution

FAQ

Does the R630 support automatic agent detection or digital concentration readout?
No. Concentration is set manually via calibrated vaporizer dials and verified using external reference analyzers per institutional QA protocols.

Is the CO2 absorber compatible with soda lime and baralyme alternatives?
Yes—the 2.1 L chamber accepts standard granular absorbents meeting ASTM D5084 specifications; calcium hydroxide-based formulations are recommended for optimal moisture retention and CO2 capture efficiency.

Can the R630 be used with wall-mounted oxygen supplies?
Yes—supplied with a standard CGA 540 oxygen pressure regulator; compatible with both cylinder and pipeline sources delivering 30–55 psi inlet pressure.

What maintenance intervals are recommended for vaporizer recalibration?
Annual laser calibration verification is advised per ISO 80601-2-13 Annex DD; more frequent checks are required if exposed to mechanical shock, solvent exposure, or extended storage above 35 °C.

Are breathing circuits supplied sterilized or ready-for-use?
Circuits are provided clean and packaged; terminal sterilization (e.g., ethylene oxide or autoclaving at ≤121 °C) must be performed by the end user per institutional biosafety policies.

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