FDA device listing

0-05-0065-U,0-05-0066-U,0-05-0071,0-05-0072-U,0-05-0073-U,0-05-0074-U,0-05-0075-U,0-05-0076-U,0-05-0077-U,0-05-0086,0-05…

FDA device listing 1404676487 · Unimed Medical Supplies Inc

Key facts

Proprietary names 0-05-0065-U,0-05-0066-U,0-05-0071,0-05-0072-U,0-05-0073-U,0-05-0074-U,0-05-0075-U,0-05-0076-U,0-05-0077-U,0-05-0086,0-05-0087,0-05-0088,0-05-0089,0-05-0102,0-05-0104,0-05-0105,0-05-0106,0-05-0107,0-05-0108,10085,10086,10110,10234,10279,10320,10327,13001,15244A-C,2025248-001-C,21027S,2104180-002-C,2312S,2312S.ED,2319P,2326P,2340S.ED,2385P-Z,24155P,24155P-I,2479S,2512S,2540S.ED,2596P,2598S,2609P,260…
Owner/operator Unimed Medical Supplies Inc
Owner/operator number 10027206
Product codes IKD
Device names IKD - Cable, Electrode
Device class Class II
Classification regulations (21 CFR) 890.1175
Review panels Physical Medicine
Registered establishments UNIMED MEDICAL SUPPLIES INC
Establishment registrations 3007307487
FEI numbers 3007307487
Establishment operations Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device listings