After the implementation of the new 2025 version of the "Customs Tax Collection and Management Reform Plan," the credit guarantee model of professional agencies has fundamentally transformed the import of medical devices. Taking a red light therapy device with a wavelength of 630nm as an example, for a single unit with an import value of approximately $120,000, the traditional model requires freezing funds up to 30% of the value, while the new agency model enables a zero-deposit operation throughout the entire process.
The Three Core Principles of the No-Deposit Agency Model
AEO Advanced Certified Enterprise Shared Credit Line
The maximum guarantee amount for a single ticket can reach up to 5 million yuan.
Annual revolving usage does not occupy the enterprise's credit line.
Principle 2: Innovative Application of Tariff Guarantee Insurance
The insurance cost is only 0.3%-0.8% of traditional margin.
The frozen funds will be released immediately upon the policy taking effect.
Support installment payment of insurance premiums
Principle 3: Post-Settlement of Import Process Fees
Customs duties/VAT deferred for payment within 45 days after release.
Logistics costs are included in payment term management.
Document handling fees will be settled based on actual occurrences.
The Five Key Steps of the Operational Process
Qualification pre-review stage
Medical Device Registration Certificate Filing Verification
Confirmation of Special Regulatory Requirements for Place of Origin
Customs clearance solution design
Accurate HS Code Classification (9018.1290)
Intelligent Matching of Regulatory Certificates (CFDA/NMPA)
Credit Guarantee Initiation
The electronic guarantee takes effect immediately.
The insurance coverage takes effect immediately.
Physical supervision process
Electronic Transmission of Radiation Safety Certificates
Online verification of equipment parameters
Expense settlement phase
Automatically generate tax breakdown table
Multi-currency payment channel support
The Five-Dimensional Evaluation Method for Agency Selection
The special requirements for medical device imports necessitate that the agency must possess:
Customs AEO Advanced Certification qualification
Medical device import specialized qualification
At least 5 successful operation cases
Complete risk compensation mechanism
A real-time updated regulatory database
A dual safeguard system for risk prevention and control
Pre - event prevention and control:Through a triple verification mechanism consisting of pre-classification review of goods, pre-confirmation of origin, and compliance review of technical parameters, the declaration error rate is controlled below 0.2%.
Post-event relief:Establish a risk reserve pool of 2 million yuan to provide advance payment services for potential late declaration fees, late payment penalties, etc., ensuring the security of the enterprise's capital chain.
Empirical Analysis of Typical Customer Cases
A private hospital imported red light therapy equipment manufactured in Germany in March 2025, with a total value of 870,000 USD. Through professional agency services:
Saving 2.61 million yuan in margin occupation.
Reduce customs clearance time by 12 working days.
The comprehensive cost was reduced by approximately 9.7%.
Achieve early clinical deployment of the equipment