GMP-grade ultrasonic cleaning for production accessories, tablet tooling, filter mesh, sieves and glassware. SS 316L tanks, DI/PW compatible, IQ/OQ documentation.
Samarth Electronics is an ISO 9001:2015 certified pharma ultrasonic cleaner manufacturer in India and a direct pharma ultrasonic cleaner exporter to Sri Lanka. Buyers looking for a reliable pharma ultrasonic cleaner supplier in Sri Lanka get factory-direct pricing, a machine built for 230 V / 50 Hz, and complete export documentation, with no trading margin in between.
In pharmaceutical manufacturing, cleaning has to be validated. Every cleaning process must be documented and must remove residues consistently below the plant's acceptance limits. Ultrasonic cleaning is reproducible: the same frequency, temperature and time give the same result every cycle. That makes it a strong fit for a validated cleaning SOP under WHO GMP, EU GMP Annex 15 and Schedule M.
In Sri Lanka, our pharma ultrasonic cleaner is used by pharma manufacturers around Colombo; QC labs of pharma and export food companies; and research institutes in Colombo and Kandy. Export units for Sri Lanka are built for 230 V / 50 Hz and shipped by sea from Nhava Sheva (JNPT) to Colombo, or by air to Colombo, with a commercial invoice, packing list, certificate of origin and technical datasheets.
Samarth Electronics' pharma-grade cleaners are built with the features QA teams check during equipment qualification. These include SS 316L electropolished tanks, DI/purified-water connections, a sloped floor with a full-bore drain (no dead legs), a calibrated PID temperature controller, and IQ/OQ protocol templates.
See the full product range on our Ultrasonic Cleaner for Pharma Industry page, or all equipment we supply in Sri Lanka.
Pharma manufacturers around Colombo use it for tablet tooling, change parts and filter mesh.
QC labs of pharma and export food companies use it for QC glassware and small lab tools.
Research institutes in Colombo and Kandy use it for R&D glassware and formulation equipment.
Ra ≤ 0.8 μm GMP surface finish, with material traceability.
DI or purified-water inlet and drain connections. WFI-compatible construction on request.
PID controller with a NABL-traceable sensor calibration certificate for batch records.
IQ and OQ protocol templates, material certificates and wiring diagrams supplied.
Sloped tank floor and full-bore drain for complete drainage between cycles.
Digital timer and set temperature give the same cleaning result every cycle.
| Frequency | 40 kHz |
| Tank material | SS 316L electropolished, Ra ≤ 0.8 μm |
| Temperature control | Calibrated PID, NABL-traceable sensor |
| Water | DI / PW inlet and drain connections |
| Drainage | Sloped floor, full-bore drain, no dead legs |
| Documentation | IQ/OQ templates, material certificates, calibration records |
| Tank sizes | 2 L lab to 50 L production accessories |
| Standards | Designed for WHO GMP, EU GMP Annex 15, Schedule M, 21 CFR use |
Specifications may vary by model and custom configuration. Confirm with our team before ordering.
| Requirement | Recommended | Notes |
|---|---|---|
| QC lab glassware & small tools | 2–10 L bench-top | SS 316L, DI rinse |
| Tablet tooling (punches & dies) | 15–30 L | Tool-holding basket, rust-preventive rinse |
| Filter mesh, sieves, change parts | 30–50 L | Large tank, full-bore drain |
| High-volume production accessories | Multi-stage system | Wash–rinse–dry with documentation |
Yes. It is accepted as part of a validated cleaning process under WHO GMP, EU GMP Annex 15, Schedule M and 21 CFR. The equipment needs the right design features (SS 316L tank, calibrated instruments, no dead legs), and the process must be qualified through IQ/OQ/PQ.
SS 316L material test reports, a NABL-traceable temperature sensor calibration certificate, IQ and OQ protocol templates, a declaration of conformity and wiring diagrams. FAT protocols are available on request.
Yes. Pharma units have DI/PW-compatible connections and SS 316L wetted parts, so no incompatible material touches the purified water. WFI-grade construction is available for sterile areas.
IQ verifies the installation. OQ verifies that every parameter stays in range. PQ shows three consecutive successful runs that remove residue below your acceptance limit, checked by swab or rinse sampling. We supply the IQ/OQ templates.
Units are built for 230 V / 50 Hz and shipped by sea from Nhava Sheva (JNPT) to Colombo, or by air to Colombo. Each shipment includes a commercial invoice, packing list, certificate of origin and technical datasheets.
Call or WhatsApp +91 9320240250 / +91 9322916496, email response@ultrasoniccleanersmfgr.com, or use our online enquiry form. Tell us your application, sample or part size and daily quantity, and we will send a quotation with the recommended model.
See all ultrasonic cleaners & lab equipment we supply in Sri Lanka »
Tell us your application, sample or part size and daily quantity. Our engineers will recommend the right model and send a factory-direct quotation.