HS code 3822 covers diagnostic kits, laboratory reagents, and chemical analysis products. These attract BCD 10% and IGST 12%, giving a total effective duty of approximately 24%. CDSCO registration is mandatory for IVD (In Vitro Diagnostic) devices.
Quick answer: HS code 3822 covers diagnostic kits, laboratory reagents, and chemical analysis products. BCD: 10%. IGST: 12%. Social Welfare Surcharge: 10% of BCD. Total effective duty: approximately 24% on CIF value. CDSCO registration is mandatory for IVD devices. Cold-chain handling may be required for temperature-sensitive reagents.
HS code 3822 covers diagnostic or laboratory reagents on a backing and prepared diagnostic or laboratory reagents. 38220090 covers diagnostic kits for lab use. 38220010 covers diagnostic kits for medical use. 38210000 covers culture media. IVD diagnostics are regulated as medical devices in India.
Medical devices use HS 9018. Pharmaceuticals use HS 3004. Chemicals use HS 28–38 depending on composition. Antibodies (research grade) use HS 3002. Correct classification between diagnostic kit (3822) and medical device (9018) affects both duty and CDSCO requirements.
Related resources: find HS codes for other products, medical device import guide.
Total effective duty on CIF value = BCD + SWS (10% of BCD) + IGST on (CIF + BCD + SWS). For HS code 3822, BCD is 10% and IGST is 12%.
| Duty Component | Rate | On ₹500,000 CIF (diagnostic kit batch) |
|---|---|---|
| Basic Customs Duty (BCD) | 10% | ₹50,000 |
| Social Welfare Surcharge (SWS) | 10% of BCD | ₹5,000 |
| IGST | 12% | ₹66,600 |
| Total Customs Duty | ~24.3% of CIF | ₹121,600 |
Note: IVD diagnostics are regulated as medical devices in India. CDSCO Class B or C registration is required depending on application and risk level.
Diagnostic kits and reagents used in export-oriented production may qualify for the Advance Authorisation scheme. Life-saving diagnostic devices on the exemption notification may attract 0% BCD.
Use our import duty calculator to compute exact landed cost for your shipment.
CDSCO registration is mandatory for IVD (In Vitro Diagnostic) devices. Class B IVDs take 3–6 months; Class C take 6–12 months. Research-use-only reagents may be exempt with proper documentation.
IVD diagnostic devices (blood glucose meters, COVID test kits, clinical chemistry reagents, etc.) are regulated as medical devices under CDSCO. They require device registration and Import Licence (Form MD-15). Class B IVDs take 3–6 months; Class C (higher risk) take 6–12 months.
Many diagnostic reagents and IVD kits require cold-chain handling (2–8°C refrigerated or -20°C frozen). Sea Air Cargo Systems arranges temperature-controlled packaging, monitored air freight, and refrigerated last-mile delivery.
Reagents strictly for research use (not clinical diagnosis) may be exempt from CDSCO device licensing but require clear 'Research Use Only — Not for Diagnostic Use' documentation.
Need help with compliance? check your compliance requirements or read our customs clearance guide.
Typical lead time: 4–14 months including CDSCO registration (3–12 months) plus shipping.
Our customs clearance guide explains each step in detail. For Bengaluru-bound cargo, we clear at BLR airport (6–12 hours for green channel air freight) or ICD Whitefield (2–4 days for sea freight).
Diagnostic kits and laboratory reagents (HS 3822) attract BCD 10%, SWS 1%, and IGST 12% — total effective approximately 24% on CIF value. IVD (In Vitro Diagnostic) kits used in clinical settings may qualify for lower IGST (5%) under the medical device concession notification.
Yes. IVD diagnostic devices (blood glucose meters, COVID test kits, clinical chemistry reagents, etc.) are regulated as medical devices under CDSCO. They require device registration and Import Licence (Form MD-15). Class B IVDs take 3–6 months; Class C (higher risk) take 6–12 months.
Many diagnostic reagents and IVD kits require refrigerated storage (2–8°C) or frozen storage (-20°C or -80°C). Sea Air Cargo Systems arranges IATA CEIV Pharma-certified cold chain for diagnostics: temperature-controlled packaging at origin, temperature-monitored air freight, and refrigerated last-mile delivery.
Reagents strictly for research use (not clinical diagnosis) may be exempt from CDSCO device licensing but require declaration of intended use. Mislabelling RUO materials as clinical products triggers compliance scrutiny. Import under clearly marked 'Research Use Only — Not for Diagnostic Use' documentation.
PCR reagents: HS 3822. ELISA kits: HS 3822. Cell culture media: HS 3821. Antibodies (research grade): HS 3002. Flow cytometry reagents: HS 3822. Most laboratory diagnostic consumables fall under HS 3822 with 10% BCD and 12% IGST.
Get exact duty calculation, compliance check, and a freight quote in 2 hours.