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2026 Domestic Industrial Chain Supply-demand & Domestic Substitution Analysis Of Import PEM Parts For Medical Device Sheet Metal Press-fit Fasteners

2026 Domestic Industrial Chain Supply-demand & Domestic Substitution Analysis Of Import PEM Parts For Medical Device Sheet Metal Press-fit Fasteners

Export volume of domestic in-vitro diagnostic and minimally invasive NMR imaging equipment expands sharply in 2026, driving synchronous demand growth of supporting medical-grade SUS316L non-magnetic press-fit parts. High-end medical sheet metal chassis previously relied on imported PEM US UNF micro press parts via Hong Kong transit with long delivery cycle and high procurement cost. In recent two years, domestic press-fit manufacturers break through non-magnetic passivation and low-carbon SUS316L wire cold heading processes, and compliant domestic medical press-fit parts realize mass substitution gradually. This article analyzes full-chain upstream & downstream raw material, quality control and certification status of medical press-fit parts, and objectively compares advantages & disadvantages of domestic and imported products.

1. Core Indicator Comparison Between Domestic Medical Press-fit Parts & Original Imported PEM UNF Press Parts

Comparison Item Domestic SUS316L Medical Non-magnetic Press Parts Original Imported PEM UNF Press Parts
Base Material Carbon Content ≤0.035% ≤0.030%
Saturated Magnetic Permeability ≤1.08 ≤1.05
48h Saline Biocompatibility Precipitation No Heavy Metal Precipitation No Heavy Metal Precipitation
Unit Procurement Cost 58%~68% Of Import Price High Benchmark Price
Standard Delivery Cycle 5~10 Days Spot Goods 20~35 Days Via Hong Kong Transit

2. Demand Characteristics Of Two Core Incremental Terminals For Medical Press-fit Parts

1. NMR & MRI imaging equipment: Mandatory saturated magnetic permeability ≤1.08, only low-carbon SUS316L non-magnetic press-fit parts are applicable; ordinary SUS304 stainless parts are eliminated directly due to high magnetism, low magnetic test report is required for every batch. 2. In-vitro diagnostic test chassis: ISO10993 biocompatible passivation and halogen-free control are required, compliant domestic press-fit parts can replace imported UNF models to greatly shorten complete machine delivery cycle.

3. Compliant Cost Reduction Plan For Press-fit Part Procurement Of Medical Sheet Metal Factories

1. Non-NMR in-vitro diagnostic equipment: Fully switch to compliant domestic medical press-fit parts meeting biocompatibility and RoHS halogen-free requirements with over 30% procurement cost reduction; 2. NMR imaging equipment: Prioritize high-end domestic ultra-low magnetism SUS316L press-fit parts, only reserve original imported PEM parts for a small number of key positions in core imaging area; 3. Lock full-set compliance documents including ISO10993 and MSDS from suppliers in advance to avoid delivery delay caused by missing component certificates during complete machine CE/MDR certification.

4. H2 2026 Medical Press-fit Industrial Chain Development Forecast

Continuous capacity release of low-carbon SUS316L fine drawn wire leads to slight downward raw material cost; domestic press-fit manufacturers equipped with full non-magnetic passivation and biocompatibility testing laboratories achieve fastest order growth; US UNF ultra-fine thread precision forming craft keeps maturing, domestic substitution ratio of imported PEM parts will break 45%; overseas medical equipment EPC gradually open access for compliant domestic press-fit parts.

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