GMP-grade ultrasonic cleaning for pharmaceutical manufacturing - glassware, production accessories, filter mesh, tablet press tooling, vial closures. SS316L electropolished tank, DI/PW compatible, calibrated temperature monitoring, IQ/OQ documentation. WHO GMP, EU GMP Annex 15, and CDSCO Schedule M compliant. Exported to pharma companies in UK, Ireland, Germany, and USA.
Pharmaceutical cleaning must be validated โ every process documented to show consistent residue removal below MACO limits. Ultrasonic cleaning, with its inherent reproducibility (same parameters = same result, every cycle), is accepted under WHO GMP, EU GMP Annex 15, CDSCO Schedule M (India), and 21 CFR Parts 211/820 as part of a validated cleaning SOP.
Our GMP-grade systems feature SS316L electropolished tanks (Ra โค 0.8 ฮผm), DI/PW water compatible connections, calibrated PID temperature controllers with NABL-traceable certificates, complete drainage (no dead legs), and IQ/OQ protocol documentation templates โ all the design requirements that pharma QA teams check during equipment qualification, built in as standard.
Ra โค 0.8 ฮผm โ GMP surface finish standard. Full material mill traceability supplied with every unit.
DI water inlet/outlet. WFI-compatible on request. No incompatible materials in the purified water circuit.
NABL-traceable calibration certificate for temperature sensor โ required for GMP process batch records.
IQ and OQ protocol templates, SOPs, and material certs supplied as standard with every pharma-grade unit.
Sloped tank floor and full-bore drain โ complete drainage between cycles (mandatory GMP design requirement).
Digital timer, set temperature, and run records compatible with Chiller Sonicator Printer for full GLP records.
| Parameter | Specification |
|---|---|
| Frequency | 40 kHz |
| Tank material | SS316L electropolished Ra โค 0.8 ฮผm |
| Temperature control | Calibrated PID; NABL-traceable sensor |
| DI water | DI/PW inlet + drain connections |
| Drainage | Sloped floor, full-bore drain, no dead legs |
| Documentation | IQ/OQ templates, material certs, calibration records |
| Tank sizes | 2L lab to 50L production accessories |
| Standards | WHO GMP, EU GMP Annex 15, Schedule M India, 21 CFR |
Used by pharmaceutical manufacturers, CMOs, API producers, and QC labs in Mumbai, Hyderabad, Ahmedabad, Baddi. Exported to pharma companies in UK, Ireland, Germany, USA, and UAE.
Samarth Electronics exports Ultrasonic Cleaner for Pharmaceutical Industry to buyers in 12+ countries. Every unit is built at your destination voltage (110V/220V/230V/400V), IEC certified, and ships with full technical documentation, CE declaration where required, and certificate of origin for preferential trade duty treatment.
Since 2006 โ thousands of units delivered across India and 12+ export countries.
Full IEC electrical certification. CE-compatible designs available for European buyers.
Every unit built to your specification โ tank size, frequency, voltage, automation level.
Material certs, calibration records, IQ/OQ protocols, CE declarations โ all supplied.
Parts dispatched to any country within days. Remote technical support always available.
No distributor markup โ 40-60% below European brands for equivalent IEC-certified quality.
Tell us your application, quantity, and destination. Our engineers respond within 24 hours with a complete quotation โ no obligation.
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