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 based in Ambarnath, Maharashtra, and a direct pharma ultrasonic cleaner supplier in Hyderabad. As an established pharma ultrasonic cleaner exporter, we build the same equipment for buyers in the UAE, Saudi Arabia, Bangladesh, Nepal, Kenya, Nigeria and Sri Lanka. Customers in Hyderabad get export-grade quality at factory-direct prices.
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 Hyderabad, our pharma ultrasonic cleaner is used by API and formulation plants in Jeedimetla, Bollaram, Patancheru and Pashamylaram; QC and analytical labs of Hyderabad's bulk-drug companies; and contract research organisations and R&D centres. Units are dispatched from our Ambarnath factory to Hyderabad in transit-safe packing, with installation guidance, operator training and spares support.
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 Hyderabad.
API and formulation plants in Jeedimetla, Bollaram, Patancheru and Pashamylaram use it for tablet tooling, change parts and filter mesh.
QC and analytical labs of Hyderabad's bulk-drug companies use it for QC glassware and small lab tools.
Contract research organisations and R&D centres use it for R&D glassware and formulation equipment.
Biotech and life-science companies in Genome Valley use it for process accessories and lab ware.
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.
Yes. Units are dispatched from our Ambarnath factory to Hyderabad in transit-safe packing, with installation guidance, operator training and spares support. We cover Genome Valley; Jeedimetla; Bollaram; Patancheru; Pashamylaram; and Medchal and the surrounding areas.
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 Hyderabad »
Tell us your application, sample or part size and daily quantity. Our engineers will recommend the right model and send a factory-direct quotation.