Description

The Avanos CLOG ZAPPER Enteral Feeding Tube Declogging System is a patented, ready‑to‑use kit designed to chemically loosen and clear certain clogs caused primarily by enteral feeding formulations. It restores patency without mechanical scraping and is intended for use by trained caregivers in hospital or home‑care settings. Appropriate for adult, pediatric, and neonatal patients.

Indications and Compatibility

• Helps clear blockages in enteral feeding tubes/devices primarily related to formula residues
• For NG, G, J, and low‑profile devices
• Compatible with ENFit connections
• May be less effective for clogs primarily caused by certain medications; follow clinical guidance

How It Works

An enzyme‑based, food‑grade formulation acts chemically/enzymatically to break down formula components and assist dislodgement of clogs. The solution is not a mechanical declogger. Reported to restore patency in over 75% of clinical uses for tubes clogged with enteral formulas.

Ingredient profile (food‑grade/GRAS)

• Maltodextrin
• Papain (protease)
• Alpha‑amylase
• Cellulase
• Citric acid
• Disodium phosphate dihydrate
• Ascorbic acid
• Potassium sorbate
• Sodium lauryl sulfate (surfactant)
• Disodium EDTA (metal chelator)

Kit Contents (typical)

• Two 10 mL oral syringes (one pre‑loaded with declogging powder)
• One 12 in (30 cm) enteral applicator
• Gauze pads (e.g., 2 × 4"×4")
• Instructions for Use
• Single‑patient use only; non‑sterile device

Safety and Precautions

• For enteral use only; not for intravenous use
• Allergen advisory: contains papaya (papain) and coconut‑derived ingredient(s); assess for related allergies
• Protective eyewear strongly recommended; solution may cause eye irritation upon contact
• Not made with natural rubber latex; not made with DEHP, DBP, or BBP

Storage and Shelf Life

• Store in a cool, dry place away from intense heat; keep in carton when practicable
• After reconstitution, refrigerate when not in use and use within 24 hours
• Shelf life (unopened): 1 year from date of manufacture

Regulatory and Manufacturing

• Rx only (USA)
• CE marked under 93/42/EEC as a Class I, non‑sterile device
• Manufactured in the USA under an ISO 13485–compliant quality system

Additional Notes

Pre‑mixed, pre‑measured, and pre‑loaded format is intended to save time and may help avoid tube reinsertion and placement confirmation where successful.