XL 10.0

Industrial Hemp & Cannabis Trimming Machine

COMING SOON!

INTRODUCING!

The CenturionPro XL 10.0

TRIMS
1500-1800
lbs/hr WET
TRIMS
300-360
lbs/hr DRY
REPLACES
350-400
Human Workers

Meet the latest innovation from CenturionPro Solutions – the XL 10.0! This industrial trimmer is shattering records with its up to 1,800 lb wet / 360 lb dry PER HOUR throughput! A beast of a machine, this system produces 250,000 cuts per minute and can replace up to 350-400 human trimmers. The industry leading power of the XL 10.0 provides continuous duty operation and reliability to tackle even the most demanding of harvests.

With variable speed control on all aspects (tumblers, blades, leaf collector and conveyor), available angle adjustments and an adjustable diverter, the XL 10.0 gives you total control over the trimming process. In addition, the kief collection system separates the trim and kief from the bud allowing for further processing and profits.

The complete customizability of this system grants every single grower the ability to fine tune their trimming experience and ensures the perfect trim – every time. Featuring five 1HP motors that drive the blades and tumbler along with five 7.5HP leaf collectors, the XL 10.0 has all the power an industrial cannabis or hemp operation requires. With an intimidating 23 cubic feet of tumbler volume and a powerful 20,000 CFM leaf collector, the XL 10.0 is the next level in trimming automation!

The industry leading processing capability of the XL 10.0 results in a lean workflow with just a single piece of equipment. Compliant with health and safety authorities, the XL 10.0 also comes with our standard 10 year trimmer warranty.

Initial Inventory Will be Limited – Reserve Yours Today!

XL 10.0 Pre-Order Form

GMP refers to the Good Manufacturing Practice Regulations promulgated by the US Food and Drug Administration under the authority of the Federal Food, Drug, and Cosmetic Act (See Chapter IV for food, and Chapter V, Subchapters A, B, C, D, and E for drugs and devices.) These regulations, which have the force of law, require that manufacturers, processors, and packagers of drugs, medical devices, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective. GMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, mixups, and errors. This in turn, protects the consumer from purchasing a product which is not effective or even dangerous. Failure of firms to comply with GMP regulations can result in very serious consequences including recall, seizure, fines, and jail time.

GMP regulations address issues including record keeping, personnel qualifications, sanitation, cleanliness, equipment verification, process validation, and complaint handling. Most GMP requirements are very general and open-ended, allowing each manufacturer to decide individually how to best implement the necessary controls. This provides much flexibility, but also requires that the manufacturer interpret the requirements in a manner which makes sense for each individual business.

GMP is also sometimes referred to as “cGMP”. The “c” stands for “current,” reminding manufacturers that they must employ technologies and systems which are up-to-date in order to comply with the regulation.