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Pharmaceutical Magnetic Iron Remover Self Cleaning Liquid Pipeline Magnetic Separator For Sale

Pharmaceutical Magnetic Iron Remover Self Cleaning Liquid Pipeline Magnetic Separator For Sale

Brand Name: M.Y
Model Number: MYZQL
MOQ: 1
Price: 1-50000 USD
Payment Terms: Prepay 30%,70% of payment before shipping
Supply Ability: >100
Detail Information
Place of Origin:
CHINA
Certification:
ISO
Adaptable Cleanliness Level:
Class 10,000 / Class 100,000 Clean Workshop
Cleaning Method:
Power-Off Demagnetization + Scraper Cleaning + High-Pressure Backwashing
Material Of Contact Parts:
316L Stainless Steel (Mirror Polishing), No Magnetic Residue
Applicable Materials:
Powder, Granules, And Small Block Materials
Parameter Name:
Specification Range
Place Of Origin:
China
Packaging Details:
Export Wooden
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Product Description

Pharmaceutical Special - Self-Cleaning Liquid Pipeline Magnetic Separator 

Pharmaceutical Magnetic Iron Remover Self Cleaning Liquid Pipeline Magnetic Separator For Sale 0

Core Product Advantages

1. Compliant with GMP Clean Requirements: Full closed structure design, no dust leakage, no hygiene dead corners. Material-contacting parts are made of 316L stainless steel with mirror polishing, resistant to high-temperature sterilization (121℃), suitable for use in clean workshops (Class 10,000 / Class 100,000) in the pharmaceutical industry.
2. Precise and No Impurity Contamination: Through high-intensity magnetic field, it adsorbs trace ferromagnetic impurities in pharmaceutical liquids, pharmaceutical intermediates. The automatic cleaning process has no material residue, eliminating impurity contamination of pharmaceutical finished products and ensuring drug safety and effectiveness.
3. Continuous and Stable Operation: Automatic cleaning requires no shutdown, and it can be connected in series to pharmaceutical liquid conveying and preparation filling production lines, avoiding production interruption and batch contamination caused by shutdown and disassembly, adapting to the continuous and standardized production needs of the pharmaceutical industry.
4. Traceable and Easy to Verify: Supports linkage with GMP management system of pharmaceutical workshops, capable of recording cleaning time, iron removal effect and equipment operation parameters, providing complete verification documents to help customers pass GMP certification audits.

Application Case Introduction

A well-known domestic pharmaceutical enterprise, producing pharmaceutical intermediates and oral liquid preparations for export to European, American, Japanese and Korean markets, previously faced batch contamination due to shutdown and disassembly of traditional magnetic separators, and could not meet the traceability requirements of GMP clean production, resulting in blocked overseas certification. After adopting the pharmaceutical-grade self-cleaning liquid pipeline magnetic separator (electromagnetic model) from Tianjin Minyang Machinery, the equipment was installed in the pharmaceutical intermediate conveying pipeline. Through the combined mode of power-off demagnetization and scraper cleaning, it is automatically cleaned every 3 hours, with an iron removal rate of 99.9%, capable of removing 0.05μm-level trace iron impurities. The equipment supports parameter recording and traceability, and can provide complete installation qualification (IQ), operational qualification (OQ) and performance qualification (PQ) documents, successfully helping the customer pass European and American GMP certifications. The equipment operates continuously without batch contamination, increasing production efficiency by 20%, and the overseas export volume of oral liquid preparations increases by 30%.

Company Profile

Tianjin Minyang Precision Machinery Co., Ltd. is a high-tech enterprise focusing on the R&D, production, sales and service of magnetic application equipment, with years of experience in the magnetic separation technology field. Headquartered in Tianjin Binhai New Area, the company has a 3,500-square-meter modern factory (including a 2,700-square-meter production workshop) and a branch in Kunming, Yunnan, providing rapid technical support and after-sales service for customers in Yunnan, Guizhou, Sichuan and surrounding areas. Since its establishment in 2019, adhering to the business philosophy of "Quality, Innovation, Service", the company integrates advanced foreign magnetic separation technology with independent R&D capabilities, holding more than 30 patents and software copyrights. It has passed ISO9001, ISO14001 and ISO45001 certifications, established a full-process quality control system, and provides GMP-compliant clean-grade magnetic separation and iron removal equipment as well as complete certification support services for the pharmaceutical industry, helping customers expand overseas pharmaceutical markets.

Product Parameter Table

Parameter Name
Specification Range
Magnetic Field Type
Electromagnetic (Demagnetizable by Power-off) / Medical-Grade Permanent Magnet
Magnetic Field Strength
7000-12000GS (Precise Adsorption of Trace Impurities)
Processing Flow Rate
2-20m³/h (Adapted to Small-Batch Precision Production in Pharmaceutical Industry)
Material of Contact Parts
316L Stainless Steel (Mirror Polishing), No Magnetic Residue
Cleaning Method
Power-Off Demagnetization + Scraper Cleaning + High-Pressure Backwashing
Adaptable Cleanliness Level
Class 10,000 / Class 100,000 Clean Workshop

Frequently Asked Questions (QA)

Q1: Can the equipment withstand high-temperature sterilization processes in the pharmaceutical industry? A1: Yes. Material-contacting parts are made of high-temperature resistant 316L stainless steel, and seals are made of high-temperature resistant silicone, adaptable to 121℃ steam sterilization. No material deformation or odor after sterilization, without affecting pharmaceutical liquid quality.
Q2: Do you provide verification documents required for GMP certification? A2: Yes. We can issue a full set of verification documents including installation qualification (IQ), operational qualification (OQ) and performance qualification (PQ), as well as material testing reports and cleanliness testing reports, helping customers successfully pass GMP certification.
Q3: Will the equipment generate noise during operation, affecting the clean workshop environment? A3: No. The equipment adopts a silent design, with an operating noise ≤60dB, complying with the noise control requirements of clean workshops, and will not affect the production environment and operators.