Where is the company located?

The company is headquartered in Nanjing, Jiangsu, China.

What shipping terms are available?

We offer various Incoterms including FOB, EXW, CFR, CIF, DDP, and DAP.

How many years has the company been exporting?

The company has been exporting since 2003, with over 15 years of experience.

CE Approved Antigen Rapid Test Kits

Name: CE Approved Antigen Rapid Test Kits
Brand: Perlong Medical Equipment Co., Ltd.
SKU: 1969802785

Jiangsu, ChinaPerlong Medical Equipment Co., Ltd.

US$2.78-3.47

1,000 Pieces

Product profile

Customization

Available

Type

Test Strips & Test Tube

Quality Guarantee Period

One Year

Model NO.

ATK-20

Group

Adult

Transport Package

Carton

Specification

50*40*38cm

Origin

China

HS Code

9000000000

Production Capacity

5000 PCS/Month

Key features

CE Approved Certification: Product holds CE approval for compliance with European safety standards.

One Year Quality Guarantee: Comes with a one-year quality guarantee period for peace of mind.

Fast Lead Time: Peak and off-peak season lead time is within 15 working days.

Global Export Experience: Exported to over 140 nations since 2003 with strong international partnerships.

Multiple Payment Options: Accepts LC, T/T, Western Union, and Money Gram for flexible transactions.

Comprehensive Product Range: Supplier offers surgical equipment, lab devices, and diagnostic reagents.

Flexible Shipping Terms: Supports various Incoterms including FOB, CIF, DDP, and DAP.

Company profile

Perlong Medical Equipment Co., Ltd.

Jiangsu, China

Business Type: Manufacturer/Factory, Trading CompanyExport Year: 2003-09-09Nearest Port: Shanghai, NingboAverage Response Time: ≤15hTerms of Payment: LC, T/T, Western Union, etc.International Commercial Terms(Incoterms): FOB, EXW, CFR, CIF, DAT, FAS, DDP, DAP, CIP, CPT, Others, FCA

AI-Powered supplier vetting

SummaryPerlong Medical Equipment Co., Ltd. is a China-based limited company in Nanjing, Jiangsu, engaged in medical-equipment trade and manufacturing. The supplier states that it has operated since 2003, possesses self-operated import and export rights, and derives 90% of sales from exports. Its product scope includes patient monitors, anesthesia, X-ray, laboratory, ECG, ultrasound, dental, ventilator, and biochemistry equipment. ISO 13485 and ISO 9001 management certifications are reported, along with 11–20 R&D engineers, 11–20 quality-control staff, and three production lines. The company claims exports to more than 140 countries and cooperation with WHO, UNDP, and UNICEF, but these claims are not independently substantiated in the provided data. The available trade records show transactions involving buyers in Uzbekistan and Tanzania, including patient-monitor shipments. Evidence is insufficient to assess financial credibility, customization capability, or the full extent of after-sales support.

Supplier typeThe supplier is identified as both a trading company and manufacturer/factory, operating as a limited company in Nanjing, China, with medical equipment as its commercial focus. Its stated product range and company profile support classification as a medical-equipment supplier with combined trading and manufacturing activities.

CertificationsThe supplier reports ISO 13485 and ISO 9001 management-system certifications. It also states that most products have obtained ISO certifications and that some have met CE and FDA requirements, although the specific certified products and certificate details are not provided.

Production capacityThe company is described as a manufacturer/factory as well as a trading company, with three production lines, 11–20 quality-control staff, and a factory location in Nanjing. Its stated manufacturing role and operating resources support production capability, although product-specific capacity and utilization are not provided.

Client casesThe supplier claims cooperation with WHO, UNDP, and UNICEF and exports to more than 140 countries. The trade records additionally identify ООО BAYMED INNOVATION in Uzbekistan and KAIRUKI HOSPITAL in Tanzania, including patient-monitor transactions; these records demonstrate named transaction cases but do not independently validate the broader international-client claims.