FDA device listing

3D Endoscope Camera: SY-UHD3000, SY-GW1100C-N,4K Endoscope Camera: SY-GW1200C-N, SY-SHREK-UHD909, YOUTAK-GW001,Endoscope…

FDA device listing 1816842009 · Anhui Shiyin Photoelectric Instrument Co., Ltd.

Key facts

Proprietary names 3D Endoscope Camera: SY-UHD3000, SY-GW1100C-N,4K Endoscope Camera: SY-GW1200C-N, SY-SHREK-UHD909, YOUTAK-GW001,Endoscope Camera: SY-GW800C-N, SY-GW900C-N, SY-GW1000C-N, SY-SHREK-7812, SY-SHREK-7815, SY-SHREK-7817, SY-SHREK-7818,Portable Endoscope Camera Unit: SY-UHD627, SY-GW621, SY-GW617, SY-GW605N, SY-GW605, SY-GW612 , SY-GW901, SY-GW902,Portable USB Endoscope Camera: SY-GW702C, SY-HD7021…
Owner/operator Anhui Shiyin Photoelectric Instrument Co., Ltd.
Owner/operator number 10084579
Product codes FWF
Device names FWF - Camera, Television, Endoscopic, Without Audio
Device class Class I
Classification regulations (21 CFR) 878.4160
Review panels General & Plastic Surgery
Registered establishments Anhui Shiyin Photoelectric Instrument Co., Ltd.
Establishment registrations 3013831261
FEI numbers 3013831261
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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