Register Your Physical Medicine Device in Colombia
Rehabilitation equipment, therapy devices, prosthetics, orthoticsโstreamlined INVIMA registration for PM&R products.
Free consultation โข No commitment required
60-180
Days to Market
500+
Devices Registered
60-80%
Cost Savings
5yr
Registration Validity
Physical Medicine Covers Therapeutic and Assistive Devices
Specialized devices need specialized expertise
Therapeutic Claims
Rehabilitation devices with therapeutic claims need clinical evidence supporting efficacy.
Electrical Stimulation
TENS, EMS, and neuromuscular stimulation devices require comprehensive electrical safety documentation.
Custom Device Complexity
Prosthetics and orthotics with custom elements need special registration considerations.
We Specialize in Physical Medicine Devices
Pure Global experts know your device category inside out
Deep Category Expertise
Rehabilitation and therapy equipment registration
Technical Documentation Excellence
Prosthetic and orthotic device expertise
Proven Registration Track Record
Electrical stimulation device registration
Ongoing Compliance Support
Home-use therapy device registration
How It Works
Free Consultation
Share your device details. We'll confirm classification, assess your documentation, and provide an exact quote.
Expert Dossier Preparation
Our regulatory specialists prepare your complete submission with deep specialty knowledge.
Submission & Management
We submit on your behalf and manage the entire review process, including deficiency responses.
Market Your Device
Receive your registration. Your device is legally marketable for 10 years.
Trusted by Leading Physical Medicine Companies
โOur rehabilitation robotics line is now in Colombian clinics thanks to Pure Global's expertise.โ
Dr. Daniel Martinez
Regulatory Affairs Director, RehabTech Systems
Transparent Pricing
Complete service, no hidden fees
Starting from
Starting from $2,000/year
Based on device class and complexitySave 60-80%
Ready to Register Your Physical Medicine Device?
Get a free consultation with our regulatory experts. We'll assess your device and provide an honest timeline and quote.