FDA device listing

ERBECRYO® 2 1-pedal footswitch,ERBECRYO® 2 Cart,ERBECRYO® 2, Cryosurgical unit,Exhaust gas hose,Extension cable,Flexible…

FDA device listing 1723951465 · ERBE ELEKTROMEDIZIN GMBH

Key facts

Proprietary names ERBECRYO® 2 1-pedal footswitch,ERBECRYO® 2 Cart,ERBECRYO® 2, Cryosurgical unit,Exhaust gas hose,Extension cable,Flexible Cryoprobe,Flexible gas hose,Gas bottle adapter,Switching valve with 2 adapters
Owner/operator ERBE ELEKTROMEDIZIN GMBH
Owner/operator number 8010173
Premarket submissions K190651
Product codes GEH
Device names GEH - Unit, Cryosurgical, Accessories
Device class Class II
Classification regulations (21 CFR) 878.4350
Review panels General & Plastic Surgery
Registered establishments ERBE Elektromedizin GmbH, ERBE ELEKTROMEDIZIN GMBH
Establishment registrations 9610614, 3009762450
FEI numbers 3002806920, 3009762450
Establishment operations Manufacturer, Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 1–9 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes 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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