FDA device listing

Suction Tubes

FDA device listing 1400638733 · Bothwin (Beijing) Medical Technology Co., Ltd.

Key facts

Proprietary names Suction Tubes
Owner/operator Bothwin (Beijing) Medical Technology Co., Ltd.
Owner/operator number 10085916
Product codes MDM
Device names MDM - Instrument, Manual, Surgical, General Use
Device class Class I
Classification regulations (21 CFR) 878.4800
Review panels General & Plastic Surgery
Registered establishments Bothwin (Beijing) Medical Technology Co., Ltd.
Establishment registrations 3025376090
FEI numbers 3025376090
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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