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ReNew 3909

by Microline Surgical, Inc.

ReNew 3909 is a Class II device made by Microline Surgical, Inc., listed in FDA GUDID since 13 Nov 2017 (UDI-DI 00811099010647), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00811099010647 UDI-DI Date13 Nov 2017ListedStatusListed 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  • Withdrawn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
ReNew
Generic name
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable
Model / Ref / Catalog
3909
Primary DI / UDI-DI
00811099010647
FDA product code
GEI
GMDN term
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endoscopic electrosurgical handpiece/electrode, monopolar, reusable

Other devices from Microline Surgical, Inc.

  • ReNew 3412

    Class II

  • ReNew 3362

    Class II

  • ReNew 3946

    Class II

  • ReNew 3411

    Class II

See all devices from Microline Surgical, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)