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PlasmaBlade™ PS300-002

by Medtronic Navigation Inc.

PlasmaBlade™ PS300-002 is a Class II device made by Medtronic Navigation Inc., listed in FDA GUDID since 18 May 2020 (UDI-DI 00643169937949), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00643169937949 UDI-DI Date18 May 2020ListedStatusListed 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  • Withdrawn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
PlasmaBlade™
Generic name
Open-surgery electrosurgical handpiece/electrode, monopolar, single-use
Model / reference
PS300-002
Primary DI / UDI-DI
00643169937949
FDA product code
GEI
GMDN term
Open-surgery electrosurgical handpiece/electrode, monopolar, single-use
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Open-surgery electrosurgical handpiece/electrode, monopolar, single-use

Similar devices in this category

Other devices filed under Open-surgery electrosurgical handpiece/electrode, monopolar, single-use.

Other devices from Medtronic Navigation Inc.

See all devices from Medtronic Navigation Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)