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ELECTROCYN soma ES5122W

by V3Bio Sdn. Bhd

ELECTROCYN soma ES5122W is a device classified as Unclassified made by V3Bio Sdn. Bhd, listed in FDA GUDID since 16 Jul 2026 (UDI-DI 09551012610479), 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 Number09551012610479 UDI-DI Date16 Jul 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  • Withdrawn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 / reference
ES5122W
Primary DI / UDI-DI
09551012610479
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)