vatican High Flux Cartridge Filters LOPAC PLUS HC

LOPAC PLUS HC high flux filters are made of PES membrane material for efficient liquid filtration. They have good hydrophilicity and low protein adsorption. The LOPAC PLUS HC prefilter features a double-layer asymmetric PES membrane, offering higher flow rate and loading capacity compared to the LOPAC HC. They are suitable for the pre-treatment of process fluids to remove impurities.

Product Description

LOPAC PLUS HC high flux filters are made of PES membrane material for efficient liquid filtration. They have good hydrophilicity and low protein adsorption. The LOPAC PLUS HC prefilter features a double-layer asymmetric PES membrane, offering higher flow rate and loading capacity compared to the LOPAC HC. They are suitable for the pre-treatment of process fluids to remove impurities.

 

Advanced Bio-Pharma Filtration Solutions

Enhance yield and ensure compliance with Feature-Tec’s precision-engineered filtration technologies.

  • Targeted Applications: mAb Production, Vaccine Processing, ADC Manufacturing, & Fermentation.

  • Core Technologies: Depth Filtration, Bioburden Reduction, & Automatic Integrity Testing.

  • Expert Services: Full Process Validation & Technical Support.

International Standards & Regulatory Compliance

Feature-Tec Sterilizing-Grade Filter Certifications & Compliance

1、Core Function & Definition (Sterilizing-Grade Identity)

Standard

Description

ASTM F838

Validated to the internationally recognized "gold standard" for bacterial retention in sterilizing-grade filters

PDA TR No. 26

Establishes scientific correlation between integrity testing and bacterial retention performance

21 CFR 211.65

Compliant with FDA requirements for material safety of pharmaceutical manufacturing equipment

 

2、Biosafety & Patient Safety

Standard

Description

USP <88> / ISO 10993

Validated for biocompatibility per USP Class VI and ISO 10993 requirements

USP <85> / EP 2.6.14

Complies with bacterial endotoxin limits to support injectable product safety

ICH Q3D / USP <232>

Complies with elemental impurity control requirements

USP <788>

Complies with sub-visible particulate matter requirements for injectable quality

BPOG Protocol (2014)

Characterized per BPOG extractables protocol to support chemical compatibility assessment

 

3、Manufacturing Process & Batch Consistency

Standard

Description

ISO 11137 (VDmax)

Validated for gamma irradiation sterilization, achieving SAL 10⁻⁶ sterility assurance level

ICH Q1A (R2), Q1E

Validated through accelerated and long-term stability studies to support claimed shelf life

ISO 9001 / 13485

Certified to quality management systems, ensuring consistent product quality and full traceability

 

4、Process Operations & Performance

Standard

Description

USP <643> / <645>

Post-flush residuals comply with USP Water for Injection (WFI) quality requirements

ISTA 2A / ASTM F2096

Validated for packaging integrity to maintain sterile barrier during transportation

 

5、Regulatory & Supply Chain Compliance Statements

Standard

Description

21 CFR 177-182

Materials comply with FDA requirements for indirect food-contact materials

GMO (EC) / BSE/TSE / BPA

Supporting declarations available: Non-GMO, BSE/TSE-Free, BPA-Free (where applicable)

 

Product Features

•  The highly asymmetric double-layer PES membrane provides enhanced hydrophilicity, higher flow rate, and greater loading capacity.

•  Unique folding membrane technology with higher filtration area per unit.

•  Excellent chemical compatibility.

 

Typical Application

•  Pre-filtration for process fluids and buffers Particle removal of process fluid.

•  Particle removal of process fluids.

 

Dimensions
Parameter Disc Filters Capsule Filters Cartridge Filters
Nominal Size (in) / S / 2.5" / 5" / 10" 2.5" / 5" / 10" / 20" / 30" (φ63/φ70)
Filtration Area (Single Layer) 3.5cm² / 20cm² S: 180cm²; 2.5": 0.073m²; 5": 0.23m²; 10": 0.63m² φ63: 2.5":0.11/5":0.23/10":0.45/20":0.90/30":1.35m²φ70: 2.5":0.15/5":0.30/10":0.60/20":1.20/30":1.80m²
Filtration Area (Double Layer) 3.5cm² / 20cm² S: 160cm²; 2.5": 0.065m²; 5": 0.20m²; 10": 0.60m² φ63: 2.5":0.11/5":0.23/10":0.45/20":0.90/30":1.35m²φ70: 2.5":0.15/5":0.30/10":0.60/20":1.20/30":1.80m²
Pore Size 0.65+0.65μm 0.65+0.65μm 0.65+0.65μm
Materials of Construction PP support/end cap/adaptor; Silicon/Fluoroelastomer/EPDM/FEP+FKM seal; Adhesive-free hot-melt; PES membrane PP support/end cap/adaptor; Silicon/Fluoroelastomer/EPDM/FEP+FKM seal; Adhesive-free hot-melt; PES membrane PP support/end cap/adaptor; Silicon/Fluoroelastomer/EPDM/FEP+FKM seal; Adhesive-free hot-melt; PES membrane
Max Forward ΔP 5bar (72.5psi) @20°C L/M: 5bar@20°C / 3bar@50°CS: 4bar@20°C / 2bar@50°C 5bar@20°C / 2bar@80°C
Max Reverse ΔP 2bar (29psi) @20°C 2bar@20°C / 1.5bar@50°C 2bar (29psi) @20°C
Component Material Toxicity Meets USP<88> Biological Reactivity for Class VI Meets USP<88> Biological Reactivity for Class VI Meets USP<88> Biological Reactivity for Class VI
Bacterial Endotoxin Aqueous extraction <0.25 EU/mL (USP<85> compliant) Aqueous extraction <0.25 EU/mL (USP<85> compliant) Aqueous extraction <0.25 EU/mL (USP<85> compliant)
Cleanness Complies with FDA 21 CFR 211.72/210.3(b)(5)(6) & USP<788> Complies with FDA 21 CFR 211.72/210.3(b)(5)(6) & USP<788> Complies with FDA 21 CFR 211.72/210.3(b)(5)(6) & USP<788>
Ingredient Material Toxicity Meets USP<88> Class VI plastics reaction test standards Meets USP<88> Class VI plastics reaction test standards Meets USP<88> Class VI plastics reaction test standards
Production Environment 100,000-class clean room 100,000-class clean room 100,000-class clean room
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