FDA device listing

First Aid kit

FDA device listing 1187582599 · Ningbo Guangbo medical Technology co.,ltd

Key facts

Proprietary names First Aid kit
Owner/operator Ningbo Guangbo medical Technology co.,ltd
Owner/operator number 10081109
Product codes OHO
Device names OHO - First Aid Kit Without Drug
Device class Class I
Classification regulations (21 CFR) 878.4014
Review panels General & Plastic Surgery
Registered establishments NINGBO GUANGBO MEDICAL TECHNOLOGY CO.,LTD
Establishment registrations 3015069920
FEI numbers 3015069920
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

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