Vileda Professional 6214R 118808 14 inch Original Roll-O-Matic Refills. SS. 12/cs
Vileda Professional 6214R 118808 — 14" Original Roll-O-Matic Stainless Steel Refills, 12/cs
The Vileda Professional 6214R (118808) are USA-made 14-inch stainless steel Roll-O-Matic® sponge mop refills designed as direct replacements for the 118550 and compatible 14-inch SS Roll-O-Matic mop heads. Sold in cases of 12, these refills are ideal for high-frequency cleanroom mopping programs in pharmaceutical, semiconductor, and medical device facilities.
Key Specifications
- Part Number: 6214R / 118808
- Refill Width: 14 inches
- Frame Compatibility: Stainless steel Roll-O-Matic mop heads
- Country of Manufacture: USA
- Quantity: 12/cs
Applications
- Replacement refills for Vileda Professional 118550 14" SS Roll-O-Matic mop
- Pharmaceutical and biotech cleanroom maintenance programs
- Semiconductor and medical device facility floor cleaning
- ISO-classified cleanroom environments
- High-frequency mop replacement programs requiring bulk refill supply
Frequently Asked Questions
Which mop head does the 6214R refill fit?
The 6214R is designed for 14-inch stainless steel Roll-O-Matic mop heads, including the Vileda Professional 118550. Always verify compatibility with your specific mop frame before ordering.
What is the difference between the 6214R and the 6210R?
The 6214R is a 14-inch refill for stainless steel mop heads. The 6210R is a 10-inch refill for stainless steel mop heads. Choose based on the width of your Roll-O-Matic mop frame.
Are these refills made in the USA?
Yes. Vileda Professional Roll-O-Matic sponge mop refills are manufactured in the USA.
How often should refills be replaced in a cleanroom program?
Replacement frequency depends on your facility's cleaning protocol, ISO classification, and disinfectant usage. Many cleanroom programs replace mop heads after each use or after a set number of cleaning cycles to maintain contamination control standards.
Are these refills autoclavable?
Please consult Vileda Professional's product documentation or your facility's validation team to confirm autoclave compatibility for your specific sterilization protocol and ISO classification requirements.
