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ReNew 3708

by Microline Surgical, Inc.

ReNew 3708 is a Class II device made by Microline Surgical, Inc., listed in FDA GUDID since 13 Nov 2017 (UDI-DI 00811099010685), 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 Number00811099010685 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  • Withdrawn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
Instrument tray, reusable
Model / Ref / Catalog
3708
Primary DI / UDI-DI
00811099010685
FDA product code
KCT
GMDN term
Instrument tray, reusable
Device class
Class II
Regulation number
880.6850
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Instrument tray, 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
  • Over-the-counter
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)