XL 5.0

Industrial Hemp & Cannabis Trimming Machine

COMING SOON!

INTRODUCING!

The CenturionPro XL 5.0

TRIMS
750-900
lbs/hr WET
TRIMS
150-180
lbs/hr DRY
REPLACES
175-200
Human Workers

The CenturionPro Solutions XL 5.0 is the little brother to our XL 10.0 beast. This smaller version of our industrial trimmer is just as impressive with a 900 lb wet / 180 lb dry hourly processing rate! This powerful machine produces 125,000 cuts per minute and can replace up to 175-200 human trimmers. The industry leading power of the XL 5.0 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 5.0 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 4 HP leaf collectors, the XL 5.0 has all the power an industrial cannabis or hemp operation requires. With an intimidating 12 cubic feet of tumbler volume and a powerful leaf collector, the XL 5.0 is the perfect industrial investment!

The industry leading processing capability of the XL 5.0 results in a lean workflow with just a single piece of equipment. Compliant with health and safety authorities, the XL 5.0 also comes with our standard 10 year trimmer warranty.

Initial Inventory Will be Limited – Reserve Yours Today!

XL 5.0 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.