Catalogue · Instruments

Microbiology & Sterilisation

Autoclaves, laminar air flow cabinets, BOD and bacteriological incubators, colony counters and aseptic handling equipment.

20 categories · 244 published records. The catalogue we can supply is broader than the catalogue we publish — send us the item if you cannot find it.

Before you order

For pharmaceutical customers the equipment is only half the purchase — the qualification documentation is the other half. GMP-specification units are supplied with IQ, OQ and PQ protocols, chamber mapping and recovery studies. Specify that requirement at enquiry stage; it changes both the model and the lead time.

Related

What laboratories usually order alongside this.

Dehydrated Culture Media

Agars, broths, bases and supplements for isolation, enumeration and identification, including pharmacopoeial formulations and vegetable-peptone media free of animal-origin raw material.

Molecular Biology

Thermal cyclers, nucleic acid extraction, transilluminators, crosslinkers, hybridisation ovens and microplate instruments.

Sample Preparation & Mixing

Magnetic and overhead stirrers, hotplates, vortex and tube mixers, homogenisers, sonicators, ultrasonic cleaners, rotary evaporators and digestion systems.

Why we publish the standard revision, not just the number.

Testing instruments are bought against a method, and a method is written against a standard. When that standard is revised, the old number stays in circulation for years — sometimes decades — because catalogues copy each other and nobody re-checks.

Three examples currently live across this industry: ASTM D1559 for Marshall stability, withdrawn in 1998. ASTM D422 for hydrometer analysis, withdrawn in 2016. IS 13311 for non-destructive concrete testing, absorbed into the IS 516 family in 2018. All three still appear on product listings you can buy from today.

That matters commercially, not just pedantically. If your quality manual cites a withdrawn standard, a NABL assessor will raise it, and the fastest way that error enters a manual is by being copied off a supplier’s specification sheet.

On qualification: for pharmaceutical customers, the documentation is half the purchase. GMP-specification equipment differs in its contact surfaces, its control system, its printed cycle records and its IQ/OQ/PQ protocol set. Specify that requirement at enquiry stage — retrofitting it after installation costs more and delays qualification.

On site preparation: compression testing machines, ductility baths, abrasion machines and large ovens need foundations, three-phase supply, drainage or extraction. We issue the foundation drawing and utility schedule with the quotation so the civil work can run in parallel with the delivery lead time rather than after it.