FDA device listing

gauze pad

FDA device listing 1270080644 · AID UNITED INTERNATIONAL CO., LIMITED

Key facts

Proprietary names gauze pad
Owner/operator AID UNITED INTERNATIONAL CO., LIMITED
Owner/operator number 9090586
Product codes NAB
Device names NAB - Gauze / Sponge,Nonresorbable For External Use
Device class Class I
Classification regulations (21 CFR) 878.4014
Review panels General & Plastic Surgery
Registered establishments AID UNITED INTERNATIONAL CO., LIMITED
Establishment registrations 3005951403
FEI numbers 3005951403
Establishment operations Foreign Exporter, 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

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