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Fecal occult blood test

I have found results from600+products and200+suppliers aboutFecal occult blood test

Commonly Used:
US$
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Type: IVD Instrument
Type: IVD Reagent
Surgical Supplies Materials
Type: Detection Card
Material: Plastic
Without Ethylene Oxide Sterilization
Quality Guarantee Period: Two Years
Group: Adult
Without Logo Printing

Sourcing guidance for Fecal Occult Blood Test

What are the key technical differences between Guaiac-based (gFOBT) and Immunochemical (iFOBT/FIT) kits?

B2B buyers should prioritize Immunochemical (FIT) kits as they are more specific to human hemoglobin, eliminating the need for dietary restrictions (like avoiding red meat) before testing. gFOBT is more cost-effective but has a higher false-positive rate due to cross-reactivity with certain foods and medications. For professional medical distribution, FIT kits with a sensitivity threshold of 50ng/mL are considered the industry standard for early colorectal cancer screening.

What international compliance standards must FOBT kits meet for cross-border trade?

As a Class II medical device, FOBT kits must possess CE Marking (IVDR) for the European market and FDA 510(k) clearance for the U.S. market. Ensure the manufacturer is certified under ISO 13485:2016, which governs the quality management systems for medical devices. Additionally, a Declaration of Conformity and Free Sale Certificate (FSC) are often required for customs clearance in many Southeast Asian and Middle Eastern regions.

How should the shelf life and storage conditions be evaluated for bulk procurement?

Standard FOBT kits typically offer a shelf life of 18 to 24 months. It is critical to verify that the buffer solution remains stable at room temperature (2°C to 30°C). Buyers should request stability testing reports from the supplier to ensure the reagents do not degrade during long-term sea freight, especially when crossing tropical climate zones.

What are the essential components of a high-quality FOBT rapid test kit?

A complete kit should include a test cassette (colloidal gold method), a sample collection tube with extraction buffer, and a patient instruction manual. For retail or home-use versions, ensure the inclusion of a paper stool catcher to improve user experience and sample accuracy. The accuracy rate should be ≥98% compared to clinical gold standards.

Cross-Border Procurement & Risk Management for Medical Diagnostics

How can I mitigate the risk of purchasing counterfeit or sub-standard medical kits?

Always verify the supplier's Business License and Medical Device Production License. Use Made-in-China.com's 'Audited Supplier' reports to check factory photos and production capacity. Request a pre-shipment inspection (PSI) by a third party like SGS or Intertek to verify that the batch numbers and expiry dates on the packaging match the certificates provided.

What are the specific shipping requirements for diagnostic reagents?

While most rapid FOBT kits do not require a strict cold chain, they must be kept in a cool, dry environment. Avoid LCL (Less than Container Load) shipping if the cargo will be exposed to high heat on a dock for extended periods. For large orders, use temperature-controlled containers or ensure the pallets are wrapped in thermal insulation blankets to prevent reagent denaturation.

How should I negotiate payment terms to ensure transaction security?

For new suppliers, avoid 100% upfront payments. A standard professional structure is 30% deposit and 70% balance against the Bill of Lading (B/L) after a successful quality inspection. Utilize Escrow services or Trade Assurance mechanisms provided by platforms like Made-in-China.com to ensure funds are only released once the shipping documents are verified.

What should be considered regarding international trade policies and customs for medical goods?

Medical supplies are subject to strict export white-list regulations in China. Ensure your supplier is on the official white-list of the China Chamber of Commerce for Import & Export of Medicines & Health Products (CCCMHPIE). Failure to provide the correct HS Code (typically 3822.00) and corresponding medical export licenses can lead to seizure by customs.

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