Consulting Wallah › Device Explorer › Other devices › Electrolytic-plasma electrosurgical system
Device Explorer · FDA GUDID · GMDN 63308

Electrolytic-plasma electrosurgical system

An assembly of devices intended to use radio-frequency (RF) alternating current in a bipolar configuration to excite electrolytes within a solution (typically saline) to create a focused, charged plasma sphere for cutting and coagulation of soft tissues during

US‑registered devices53in commercial distribution
Companies2labelers on GUDID
Single‑use87%of device records
Sterile87%labelled sterile
Prescription17%Rx‑only share
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Share of device records

Jiangsu Bonss Medical Technology Co., Ltd.4483%
Minerva Surgical, Inc.917%

Top labelers

CompanyDevicesShare
Jiangsu Bonss Medical Technology Co., Ltd.4483%
Minerva Surgical, Inc.917%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

BONSSSymphion Operative Hysteroscopy System Prime ConSymphion Operative Hysteroscopy System Prime ConSymphion Fluid Deficit ReadoutINFINITY Fluid Management AccessorySymphion Spare FootswitchSymphion Controller - RefurbishedSymphion ControllerSymphion Fluid Management AccessoriesSymphion Resecting Device

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
GEIElectrosurgical, Cutting & Coagulation & Accessories44
PGTInsufflator, Hysteroscopic, Fluid, Closed-Loop Recirculation9
HIGInsufflator, Hysteroscopic5
HIHHysteroscope (And Accessories)1

GMDN & GCC registration

  • GMDN code 63308 · non‑implantable
  • Single‑use 87% · sterile 87% · Rx‑only 17% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

How many electrolytic-plasma electrosurgical system products are registered in the US?

53 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Electrolytic-plasma electrosurgical system", from 2 companies. The largest labeler is Jiangsu Bonss Medical Technology Co., Ltd. with 83% of records.

Which FDA product codes apply?

GEI (Electrosurgical, Cutting & Coagulation & Accessories), PGT (Insufflator, Hysteroscopic, Fluid, Closed-Loop Recirculation), HIG (Insufflator, Hysteroscopic), HIH (Hysteroscope (And Accessories))

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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