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The Baseline Fold-Up Monofilament Evaluator is a 5-piece handset used to measure cutaneous sensory perception threshold. Each monofilament represents a unique amount of force, marked by force and size, providing objective and repeatable results. The fold-up nylon filament design protects the filaments during storage and transport. The set includes five sensation levels and ships in a soft-shell protective carrying case.
Occupational therapists, physical therapists, and clinicians who perform cutaneous sensory perception threshold evaluations will find the Baseline Fold-Up Monofilament Evaluator a 5-piece handset with five sensation levels (2.83, 3.61, 4.31, 4.56, and 6.65) that provides objective and repeatable results in a portable, fold-up format. Rehabilitation clinics and therapy departments that need a compact, easy-to-transport sensory evaluation tool will find the fold-up nylon filament design and soft-shell carrying case practical for clinical and field use. Research and academic settings that require standardized monofilament evaluation tools will find the Baseline 121740 a consistently available 5-piece handset with marked force and size designations. DME providers and medical supply retailers that stock Baseline evaluation tools will find the 121740 a consistently available fold-up monofilament evaluator set.
What sensation levels are included in this set?
This 5-piece set includes monofilaments at 2.83, 3.61, 4.31, 4.56, and 6.65 cutaneous sensation levels, each marked by force and size for easy identification during evaluation.
What does the fold-up design do?
The fold-up nylon filament folds back into the handle for protection during storage and transport, reducing the risk of filament damage and extending the usable life of each monofilament.
Does this set come with a case?
Yes. The set ships and stores in a soft-shell protective carrying case, keeping all five monofilaments organized and protected during transport and storage.
How are the monofilaments identified?
Each monofilament is marked with its force and size designation, allowing clinicians to quickly identify and select the correct filament during evaluation without referring to external documentation.