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SED-6RCDY-A

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SED-6RCDY-A

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SED-6RCDY-A — Dissolution Tester

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SED-6RCDY-A Intelligent Drug Dissolution Tester. 6-channel high-performance dissolution device strictly compliant with current ChP and USP specifications and data integrity requirements. Supports basket / paddle / small-

ChP (Chinese Pharmacopoeia)USPData Integrity Compliance

Délai de livraison

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Fonctionnement

Sample placed in constant-temperature dissolution vessel (ambient – 45 °C); paddle or basket rotates at 10–300 RPM dissolving the drug into the dissolution medium; water-bath circulation maintains temperature accuracy ≤ ±0.3 °C; timed sampling with rehydration cup replenishment; data automatically recorded with full audit trail.

Processus de fonctionnement

1Sample placed in constant-temperature dissolution vessel (ambient – 45 °C); paddle or basket rotates at 10–300 RPM dissolving the drug into the dissolution medium; water-bath circulation maintains temperature accuracy ≤ ±0.3 °C; timed sampling with rehydration cup replenishment; data automatically recorded with full audit trail.

Caractéristiques techniques

Caractéristiques de la variante : SED-6RCDY-A

Caractéristiques

Modèle

SED-6RCDY-A

Tension

220V 50Hz 1Φ

Puissance

1.2 kW

Dimensions

Longueur

580 mm

Largeur

540 mm

Hauteur

540 mm

Caractéristiques principales

6 channels parallel testing

Compliant with ChP / USP / data integrity requirements

Supports 5 dissolution methods: basket, paddle, small-cup, paddle-disk, cylinder

Three-level user rights management + audit trail + data backup

Test report printout / USB export

Paddle radial run-out ≤0.5 mm; basket run-out ≤1.0 mm; shaft–vessel axis deviation ≤1.0 mm

Speed 10–300 RPM, accuracy ≤ ±1%

Temperature range: ambient – 45 °C; resolution 0.1 °C; accuracy ≤ ±0.3 °C

Double over-temperature protection + temperature calibration

Appointment (scheduled) heating

Auto-centering of dissolution vessels and stirrers

Professional medical-grade water-circulation quick connectors

2 × 150 ml rehydration cups

Max runtime 999 h 59 min 59 s; ≤100 sampling time points

Fully compliant with ChP / USP and data integrity requirements

Free IQ/OQ validation documentation provided

Auto-centering + medical-grade quick connectors for easy operation

High-precision ±0.3 °C constant temperature control with double over-temperature protection

Applications

Drug dissolution rate testing

Quality research of oral solid dosage forms

GMP / data-integrity compliance testing

Secteurs

Pharmaceuticals

Drug R&D

QC/QA laboratories

SED

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Conformité

ChP (Chinese Pharmacopoeia)

USP

Data Integrity Compliance