BABIO Med | In Vitro Diagnostic Solutions | Rapid Test Kits & Medical Consumables

About BABIO Med

Founded in 2003, Jinan BABIO Biotechnology Co., Ltd. is a professional high-tech enterprise specializing in the research, development, manufacturing, and distribution of in vitro diagnostic reagents. The company was successfully listed on the National Equities Exchange and Quotations (NEEQ) in 2014 under the security name "Baibo Biotechnology" (Stock Code: 830774).

With over 72 independent intellectual property rights and 91 medical device registration certificates approved by CFDA, BABIO has established a strong presence in more than 100 countries worldwide. Our mission is to deliver accurate, reliable, and cost-effective diagnostic solutions for global healthcare providers, laboratories, and public health institutions.

2003

Founded

2014

Listed on NEEQ

100+

Countries Served

Our Product Range

Comprehensive diagnostic solutions across multiple domains including human health, veterinary care, food safety, and laboratory consumables.

SARS-CoV-2 Antigen Rapid Detection Kit

Colloidal Gold Method – Fast, accurate detection of SARS-CoV-2 antigens with BfArM and PEI compliance.

• Qualitative detection of nucleocapsid protein
• Nasal or throat swab sample
• Results in 15 minutes
• CE certified

Monkeypox Rapid Test

Immunochromatographic assay for rapid screening of Monkeypox virus antibodies in human serum or plasma.

• IgM/IgG dual detection
• Simple procedure, no equipment needed
• Shelf life: 24 months
• Room temperature storage

Virus Transport Kit (Inactivated)

Stabilizes and inactivates viral samples for safe transport and testing. Compatible with PCR and antigen assays.

• Viral inactivation within minutes
• Preserves RNA integrity
• Available with flocked swabs
• Sterile, ready-to-use format

Dehydrated Culture Medium

High-purity dehydrated media for microbial cultivation in clinical, food, and environmental testing.

• Nutrient Agar, R2A, SS Agar available
• Low contamination risk
• Batch-tested for performance
• Scalable packaging options

Feline Rapid Test Kit

POCT solutions for common feline diseases including FeLV, FIV, and Toxoplasma gondii.

• Whole blood, serum, or plasma
• 10-minute results
• High sensitivity and specificity
• Veterinary clinic compatible

Aflatoxin Rapid Test Cassette

Quantitative lateral flow assay for aflatoxin B1 in grains, feed, and food products.

• Detection limit: 1 μg/kg
• No specialized equipment
• Ideal for field testing
• Complies with EU standards

Combo SARS-CoV-2 / Flu A&B / RSV Antigen Test

Multiplex rapid test for differential diagnosis of respiratory infections.

• Single swab, three pathogens
• Clear visual results
• Reduces misdiagnosis
• Suitable for clinics and airports

Blood Collection Tube

Sterile, vacuum-sealed tubes with various anticoagulants for hematology and clinical chemistry.

• EDTA, Heparin, Serum types
• Gel separator available
• Barcode labeling option
• ISO 6009 compliant

View All Products

Why Choose BABIO Med?

Certified Quality

91 CFDA medical device registrations, CE certifications, and compliance with BfArM and PEI standards.

Global Reach

Distributed in over 100 countries with reliable logistics and multilingual support.

Innovation-Driven

72+ independent intellectual property rights and ongoing R&D in POCT and molecular diagnostics.

Expert Support

Dedicated technical team with fast response times and regulatory guidance.

Frequently Asked Questions

Are BABIO products CE certified?

Yes, many of our rapid test kits, including the SARS-CoV-2 Antigen Detection Kit, are CE certified and meet European regulatory requirements.

Can I order custom-branded kits?

Yes, BABIO offers OEM and ODM services for private labeling, packaging customization, and formulation adjustments based on client needs.

What is the minimum order quantity (MOQ)?

MOQ varies by product. For rapid test kits, it typically starts at 1,000 units. Contact us for specific product quotes.

Do you provide technical documentation?

Yes, we provide IFUs, CE declarations, 510(k) summaries (if applicable), and regulatory support for import registration.

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