Murrplastik KDL/H-VA FDA Cable Entry System Review: Specs, Price and Applications
Updated: 7 days ago
Murrplastik KDL/H-VA FDA is a cable-entry system using a stainless-steel frame and matched grommets for pre-assembled cables, intended for a defined hygienic enclosure installation rather than an electronic controller.
Quick Verdict
KDL/H-VA FDA is useful where pre-terminated cables must pass through a hygienic machine or control enclosure with a specified sealing and strain-relief arrangement. Confirm the exact frame, grommet material and cable diameters; FDA-compliant material wording does not certify an entire machine or cleaning process.
Murrplastik KDL/H-VA FDA Cable Entry System at a Glance
Product form: Stainless-steel split cable-entry arrangement for pre-assembled cables
Matched seals: KDT/X-FDA grommets are identified with the supplied configuration
Cut-out reference: Standard 16- and 24-pole connector-style cut-outs in the listing
Capacity: Up to 48 cables in the listed family; actual seal population and cable sizes govern
Listed temperature: −40 to +80 °C; confirm the selected materials and operating conditions
Protection scope: Listing states IP66; do not transfer a broader FDA-series IP69K maximum to an unspecified configuration
Price: Request a quote for the exact ordering configuration.
Technical Specifications
Specification | Documented configuration |
Product form | Stainless-steel split cable-entry arrangement for pre-assembled cables |
Matched seals | KDT/X-FDA grommets are identified with the supplied configuration |
Cut-out reference | Standard 16- and 24-pole connector-style cut-outs in the listing |
Capacity | Up to 48 cables in the listed family; actual seal population and cable sizes govern |
Listed temperature | −40 to +80 °C; confirm the selected materials and operating conditions |
Protection scope | Listing states IP66; do not transfer a broader FDA-series IP69K maximum to an unspecified configuration |
Design and Build
A split entry can preserve factory-fitted cable connectors while routing the cable through an enclosure boundary. The practical fit depends on both the outer connector and the cable's sealing diameter. Specify every cable and matched grommet, including unused positions and the actual panel cut-out. The maximum cable-count headline is not a layout for any arbitrary mixture of Ethernet, sensor, I/O and power cables.
Select an enclosure entry from the complete cable schedule and panel construction. Identify the connector envelope, cable diameter, seal type, frame and mounting hardware. Allow the cable bend and service access required on both sides. A compact entry is useful only when the installed cables and enclosure can reproduce its specified sealing and retention arrangement.
Configuration and Integration
The stainless frame and matched material address part of a hygienic installation. FDA-compliant material language should be supported by the selected component's documentation and should not become a claim that the whole cabinet or production machine is FDA approved. Likewise, hygienic design principles are distinct from a certification or validation of the user's cleaning process. Check cleaning agents, exposure and the selected seal material against the actual application.
Prepare an assembly record showing which seal belongs to each cable and how unused locations are closed. Keep power and signal routing consistent with the machine's electrical and EMC design. Follow the selected product's mounting and compression instructions. Cable entry does not replace cable support elsewhere in the installation or determine the permitted movement of a connected machine component.
Applications and Use Cases
Relevant to a specified hygienic machine enclosure or control-panel cable entry, including compatible pre-terminated sensor, I/O or communication cables. Confirm the complete frame/seal/cable arrangement and cleaning conditions.
The directory gives IP66 for this product, while a current manufacturer page discusses higher protection levels across a broader product range. This review retains the model-scoped figure and requires the exact assembled configuration to be confirmed. Panel finish, compression, cable sizing and strain relief affect the installed result. Maintain the approved cable-and-grommet schedule so later additions or replacements preserve the defined enclosure boundary.
Judge the assembly by its installed enclosure boundary, routing and serviceability. Component materials, cut-out dimensions and protection references are useful when they apply to the exact assembled configuration. Their presence in a family description does not validate a different frame, cable population or cleaning environment.
Alternatives and Selection
Compare the exact KDL/H-VA FDA assembly with matched hygienic glands and another split entry using identical cable diameters, connector sizes, enclosure cut-out and cleaning requirements. Include seal replacement and cable-change effort.
Price and Value
Price: Request a quote. The quotation should identify the exact product configuration, included options, delivery terms and support scope. Accessories and integration work should be listed separately so the hardware price can be compared on a like-for-like basis. A family name or headline specification is not a complete purchasing description.
Assess value against the work the product enables in the machine. Include the engineering needed to configure it, the equipment that must operate alongside it and the effort required to maintain or replace it. A lower component price can be outweighed by extra integration work, while additional features are valuable only when the application can use them. Compare written configurations rather than assumed package contents.
Pros and Cons
Pros
Split arrangement supports compatible pre-assembled cable installation
Stainless frame and matched grommets address a defined hygienic enclosure requirement
Configured cable density can reduce separate entry positions
Cons
Maximum cable count depends on actual grommets and cable diameters
Material compliance does not certify the complete machine or cleaning process
Sealing and strain relief depend on correct assembly and later maintenance
Who Should Consider Murrplastik KDL/H-VA FDA Cable Entry System?
KDL/H-VA FDA is useful where pre-terminated cables must pass through a hygienic machine or control enclosure with a specified sealing and strain-relief arrangement. Confirm the exact frame, grommet material and cable diameters; FDA-compliant material wording does not certify an entire machine or cleaning process.
The strongest purchasing case is a clearly defined requirement that matches the documented configuration. If the project depends on a particular option, interface or mechanical arrangement, include it explicitly in the order. Keep the accepted configuration with the equipment documentation so a later replacement preserves the intended application.
Commissioning and Acceptance
Inspect the completed entry and the documented cable/seal population against the approved installation instructions. Verify retention, access and the required enclosure and cleaning qualification through the applicable procedure. Record changes when a cable is removed, replaced or added. Maintenance should restore the specified seals and assembly condition rather than merely fill a visible opening.
Murrplastik KDL/H-VA FDA Cable Entry System FAQ
What is Murrplastik KDL/H-VA FDA Cable Entry System?
Murrplastik KDL/H-VA FDA is a cable-entry system using a stainless-steel frame and matched grommets for pre-assembled cables, intended for a defined hygienic enclosure installation rather than an electronic controller.
Which configuration is reviewed?
Product form: Stainless-steel split cable-entry arrangement for pre-assembled cables. Matched seals: KDT/X-FDA grommets are identified with the supplied configuration.
What is the main selection consideration?
KDL/H-VA FDA is useful where pre-terminated cables must pass through a hygienic machine or control enclosure with a specified sealing and strain-relief arrangement. Confirm the exact frame, grommet material and cable diameters; FDA-compliant material wording does not certify an entire machine or cleaning process.
What applications should it be considered for?
Relevant to a specified hygienic machine enclosure or control-panel cable entry, including compatible pre-terminated sensor, I/O or communication cables. Confirm the complete frame/seal/cable arrangement and cleaning conditions.
What is a documented advantage?
Split arrangement supports compatible pre-assembled cable installation. Stainless frame and matched grommets address a defined hygienic enclosure requirement.
What limitation matters during integration?
Maximum cable count depends on actual grommets and cable diameters. Material compliance does not certify the complete machine or cleaning process.
What is the price?
Price: Request a quote. Specify the exact ordering configuration, required options, accessories and delivery terms.
How should an alternative be compared?
Compare the exact KDL/H-VA FDA assembly with matched hygienic glands and another split entry using identical cable diameters, connector sizes, enclosure cut-out and cleaning requirements. Include seal replacement and cable-change effort.
Product information: Murrplastik hygienic cable-entry manufacturer description and supplied KDL/H-VA FDA listing, with model-specific sealing and material documentation required for procurement.
Pricing is quotation-based and may change. Options, availability, delivery and application requirements depend on the selected ordering configuration.
