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SED-0.6MM-J
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SED-0.6MM-J
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SED-0.6MM-J — 0.6 m³, Motorized Double-Door, High-Pressure Rating

La description complète de ce modèle est encore en cours de traduction. Consultez les détails en anglais ou demandez des informations à notre équipe. English

SED-0.6MM-J Pulsating Vacuum Sterilizer. Horizontal double-layer cabinet with airtight double-leaf motorized doors and pressure safety interlock. Inner chamber 1,050 × 680 × 850 mm; overall 1,330 × 1,400 × 1,920 mm; net

Designed and manufactured per pharma GMP standard with GMP authentication interfaceGB/T 150.1~4-2024 (Steel Pressure Vessel) compliantX-ray flaw-detection inspection with full quality certification
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Fonctionnement

Pulsating-vacuum saturated-steam sterilization. Process flow: Auto-preparation → Pulsating vacuum (water-ring pump alternates vacuum/steam to expel cold air) → Heat-up (saturated steam at 0.25 MPa raises temperature to 105–139°C; latent-heat condensation provides high-temperature wet environment for microbial kill) → Sterilization (PLC holds setpoint for programmed time) → Drying (vacuum + jacket heating) → End. Two independent Pt100 sensors monitor chamber. ASCO/CIS hydrophobic valve system prevents reverse contamination post-sterilization.

Processus de fonctionnement
1Pulsating-vacuum saturated-steam sterilization.
2Process flow: Auto-preparation → Pulsating vacuum (water-ring pump alternates vacuum/steam to expel cold air) → Heat-up (saturated steam at 0.25 MPa raises temperature to 105–139°C; latent-heat condensation provides high-temperature wet environment for microbial kill) → Sterilization (PLC holds setpoint for programmed time) → Drying (vacuum + jacket heating) → End.
3Two independent Pt100 sensors monitor chamber.
4ASCO/CIS hydrophobic valve system prevents reverse contamination post-sterilization.

Caractéristiques techniques

Caractéristiques de la variante : SED-0 this model

Caractéristiques

Modèle
SED-0.6MM-J
Tension
AC 380 V / 220 V, 50 Hz, 3-phase 5-wire
Fluides et énergie
Electricity: 380/220 V, 50 Hz, 3-phase 5-wire, 2.5 kWh per cycle. Saturated steam 0.4–0.6 MPa, ~35 kg/cycle. Water (drinking + pure) 0.1–0.3 MPa, ~200 kg/cycle. Compressed air 0.5–0.7 MPa. Cooling water for vacuum pump.
Détails de conformité
Designed per pharma GMP standard with validation interface (real-time archive, 3-level permission, audit trail). Pressure vessel: GB/T 150.1~4-2024; X-ray flaw inspected. Pneumatic-valve + trap design eliminates reverse-leak contamination. Operating range −40°C to +50°C, RH 10–93%.
Puissance
2.5 kW
Pression d’air
Compressed air 0.5-0.7 MPa; saturated steam 0.4-0.6 MPa; water 0.1-0.3 MPa; ultimate vacuum -0.095 MPa

Dimensions

Longueur
1330 mm
Largeur
1400 mm
Hauteur
1920 mm
Poids
1200 kg
Emprise au sol
Outside dimensions 1,330 (L) × 1,400 (W) × 1,920 (H) mm; net weight 1,200 kg. Inner chamber 1,050 × 680 × 850 mm. Pass-through double-leaf — install in wall between sterile and non-sterile rooms.

Matériaux

Matériaux en contact
SS304 inner chamber 6 mm welded — SS316L door plate 8 mm — SS304 sterilization sieve plate — SS304 sanitary-clamp piping — medical silicone rubber door gasket.
Matériaux du bâti
SS304 inner shell 6 mm — SS304 fully-enclosed jacket 6 mm — SS304 door rack/sawtooth — SS304 1.2 mm oil-mill drawn outer cover — 50 mm aluminum-silicate insulation.

Caractéristiques principales

Chamber 1,050 × 680 × 850 mm (~0.6 m³); 1 set 304 SS sieve plate included
Working 0.25 MPa @ 105–139°C; design 0.3 MPa @ 144°C; heat equilibrium ≤±1°C; vacuum −0.095 MPa
Inner shell SS304 6 mm welded; outer jacket SS304 6 mm — Class I pressure vessel
Door plate 8 mm SS316L; sawtooth rack SS304; pneumatic medical silicone door gasket
Double-leaf motorized doors with pressure safety interlock and self-lock
Siemens S7-series PLC + SMART touchscreen (3-level permission, audit trail)
EPSON-chip pin-printer with 10-year print archive
Ereith paperless recorder
ASCO USA angle-seat pneumatic valves (4 M cycles)
0.22 μm in-line sterile air filter (Santong Jingong)
TEMPRESS Denmark movable Pt100 + Germany B+B Pt100 soft probe
HUBA Switzerland pressure transmitter
GB/T 150.1~4-2024 compliant; X-ray inspected; GMP validation interface
Higher pressure rating (0.25 MPa working / 0.3 MPa design) — broader sterilization window 105–139°C
Premium imported probes: TEMPRESS Denmark + Germany B+B — best-in-class temperature accuracy
Audit-trail HMI with 3-level permission — pharma compliance ready
EPSON pin-printer with 10-year archive — meets long-term record retention
ASCO USA valves (4 M cycle life) — proven durability
Hydrophobic valve + trap prevents reverse contamination
GMP standard validation interface

Applications

Saturated-steam sterilization of clothing and dressings
Sterilization of metal medical/surgical instruments
Culture-medium sterilization
Glassware sterilization
Liquid-load sterilization (in-vessel probe included)

Secteurs

Hospitals
Pharmaceutical manufacturing (injectables / sterile preparations)
Health authorities and research institutes
Medical device sterilization

Marques des composants

Siemens Germany — S7-series PLC and SMART touchscreen
Beijing Weihuang (Brighten) — WH-series micro pin printer (original EPSON chip)
TEMPRESS Denmark — TR27V1 movable hard Pt100 dual-core probe (Class A, ≤0.15°C)
Ereith/Iris — WZPK fixed Pt100 dual-core probe + paperless recorder
B+B Germany — Pt100 soft probe (dual-core, Class A, ≤0.15°C)
HUBA Switzerland — pressure transmitter
ASCO USA — angle-seat pneumatic valve (4 M cycles)
Santong Jingong — 0.22 μm in-line sterile air filter
Zhongzhi CIS — float-ball steam trap
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Conformité

Designed and manufactured per pharma GMP standard with GMP authentication interface
GB/T 150.1~4-2024 (Steel Pressure Vessel) compliant
X-ray flaw-detection inspection with full quality certification

Nettoyage et entretien

Chamber inner surface: precision mechanical and chemical finishing for corrosion resistance and easy cleaning. SS304 1.2 mm oil-mill drawn outer cover wipes clean. Sanitary-clamp 304 piping with smooth, crack-free weld fittings.

Documentation

Fiche technique (PDF)
Aperçu de l’équipement, caractéristiques et dimensions · Document d’origine (anglais)
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Manuel opérateur
Installation, fonctionnement et dépannage · Document d’origine (anglais)
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Fiche comparative (Standard et Économique)
Comparaison des configurations · Document d’origine (anglais)
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Protocoles IQ / OQ / PQ
Documentation de validation pour la conformité GMP · Document d’origine (anglais)
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Protocoles FAT / SAT
Essais de réception en usine et sur site · Document d’origine (anglais)
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Plans CAD (STEP / IGES / DWG)
Plans d’ingénierie pour l’implantation · Document d’origine (anglais)
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Certificats d’étalonnage
Niveau sonore, résistance de terre, rigidité diélectrique et rugosité · Document d’origine (anglais)
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DQ (qualification de la conception)
Protocole complet de qualification de la conception · Document d’origine (anglais)
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Certificats matières
Composition de l’acier inoxydable 316L · Document d’origine (anglais)
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