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ELECTROCYN soma ES5110W

by V3Bio Sdn. Bhd

ELECTROCYN soma ES5110W is a device classified as Unclassified made by V3Bio Sdn. Bhd, listed in FDA GUDID since 2 Apr 2026 (UDI-DI 09551012610363), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number09551012610363 UDI-DI Date2 Apr 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
ELECTROCYN soma
Generic name
Antimicrobial wound irrigation solution
Model / Ref / Catalog
ES5110W
Primary DI / UDI-DI
09551012610363
FDA product code
FRO
GMDN term
Antimicrobial wound irrigation solution
Device class
U
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 500 Milliliter

Similar devices

Other devices filed under FDA product code FRO (Dressing, Wound, Drug).

Other devices from V3Bio Sdn. Bhd

See all devices from V3Bio Sdn. Bhd →

Properties

  • Prescription use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)