IVD / Professional Use Only

Better access to reliable IVD diagnostics.

Source respiratory PCR panels, infectious disease assay menus, real-time qPCR and nucleic acid extraction instruments, HbA1c analysers and immunofluorescence POCT analysers — from manufacturers screened for registrations, certifications and export track record. Final quotation, product documentation and export arrangements are provided by the contracting manufacturer or exporter.

Partner lines: CE / FDA / ISO 13485 certified 24h initial RFQ response
IVD analyser and reagent kits available for sourcing
Supplier lines in 110+ countries
Model docs in 2–5 working days
5
Product families
600+
Assays behind the menu
110+
Countries reached
24h
RFQ response

Product portfolio

Five product families. One accountable workflow.

Five product families available for qualified sourcing today, plus an expanding immunoassay and molecular-POCT pipeline available on request.

CORE LINE
Respiratory multiplex PCR panel kits and tubes
01

Respiratory & Syndromic Molecular Panels

Multiplex real-time PCR and rapid isothermal amplification assays covering the pathogens that matter in seasonal and outbreak readiness.

  • Influenza A/B, RSV, adenovirus, metapneumovirus, rhinovirus panels
  • Six-pathogen respiratory bacterial panels & atypical pneumonia
  • Dried-reagent format options for reduced cold-chain burden
~30 min
rapid isothermal option
1,000 copies/mL
analytical sensitivity (ref.)
View product scope →
CORE LINE
Real-time qPCR analysis system
02

Molecular Workflow Instruments

A closed-loop sample-to-answer workflow: partitioning, extraction, amplification and analysis — sized from clinic bench to high-throughput laboratory.

  • Real-time qPCR analysis systems (multiple throughput classes)
  • Automated extraction: 32 / 48 / 96 channels
  • Partitioning, liquid handling & workstations
9–11 min
1–96 sample extraction
2,160
samples / 24 h (ref.)
View product scope →
Infectious disease PCR assay kits
03

Infectious Disease Assay Menu

Single-target and specialty PCR assays that complete or extend an installed molecular platform — the recurring-revenue side of an instrument-led project.

  • Hepatitis B (HBV DNA), norovirus, enterovirus
  • Five-pathogen diarrheagenic E. coli panel
  • Carbapenemase / antimicrobial-resistance genes
500 copies/mL
ref. HBV detection limit
600+
assay portfolio behind menu
View assay menu →
CE · FDA
HbA1c benchtop analyser
04

HbA1c & Diabetes Management

Dual-technology HbA1c platforms from one of China's earliest IVD exporters — benchtop HPLC systems and one-step POCT analysers for clinic and ward use.

  • HbA1c benchtop analysers (HPLC technology)
  • POCT HbA1c analyser — one-step operation
  • Matching reagents, calibrators and controls
2 platforms
HPLC + POCT
CE · FDA · ISO 13485
line certifications
View product scope →
CE · FDA
Immunofluorescence POCT analyser
05

Immunofluorescence POCT

Quantitative immunofluorescence analysers and assays for emergency, ward-side and primary-care testing — a natural companion to the molecular respiratory workflow.

  • Cardiac markers: cTnI / Myo / CK-MB panels
  • Heart failure: NT-proBNP · Sepsis: PCT
  • Benchtop and portable quantitative analysers
3–15 min
quantitative results
110+ countries
export track record
View product scope →
+

On-request pipeline

Under active supplier qualification — qualified enquiries are matched first.

  • Chemiluminescence immunoassay (CLIA) platforms — EU CE-IVDR
  • Molecular point-of-care: sample-in, result-out, ~25 min
  • Tropical disease, HPV genotyping & STI menus
See pipeline status →

A clear process

From requirement to ready-to-ship.

1

Clarify the requirement

We collect the product, destination market, intended use, quantity, timing and required documentation.

2

Introduce relevant supply options

We share model-level product information and documentation availability, matched to your market's registration pathway.

3

Contract directly with the exporter

You confirm model, local requirements and transaction terms directly with the contracting manufacturer or exporter in writing.

4

Exporter manages delivery

The contracting exporter issues quotation, PI, contract and export documents. Buyers remain responsible for local registration, import clearance and market access.

Quality & documentation

Documentation that starts with the details.

Product and manufacturer documents, when available, are supplied by the contracting manufacturer or exporter for the requested model.

Product data

Specifications, packaging, storage and transport information.

Quality information

CE certificates, FDA registrations, ISO 13485 certificates and batch documentation where available.

Trade documentation

Commercial and export documents issued by the contracting exporter, where available.

Market-access boundary

Buyers confirm destination-market registration, importer obligations and local labelling before shipment.

Catalogue text is indicative. We do not represent that every product is registered, authorised or suitable for every market. Availability must be verified by the contracting manufacturer or exporter at the exact model and destination-country level.

About IVD Relay

Designed for qualified B2B conversations.

We act as an independent sourcing liaison: we clarify buyer requirements, screen supply against certification and export-track-record criteria, and facilitate introductions to potential supply partners. We are not the manufacturer, exporter of record, importer of record or destination-market regulatory representative.

Supplier screening criteria

  • NMPA registrations on flagship assays (Class III where applicable)
  • ISO 13485 quality systems; CE and/or FDA certification where available
  • Demonstrated export track record — 95 to 110+ countries across partner lines
  • In-house R&D and manufacturing (no trading-only intermediaries)
  • Willingness to provide model-level documentation to qualified buyers

Request for quotation

Tell us what you need to source.

Qualified distributors, laboratories and institutional buyers only. We respond within 24 hours on working days.

By submitting you confirm you are a professional B2B buyer. Product information is shared at the supplier's authorisation. We do not sell consumer IVD products.