Skip to content

Minder® Surgical Instrument Kit P2036354

by Epi-Minder Pty, Ltd. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840336500078 UDI-DIDate1 Dec 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Minder® Surgical Instrument Kit
Generic Name
Electroencephalographic monitoring system
Model / Ref / Catalog
P2036354
Primary DI / UDI-DI
00840336500078
FDA Product Code
SEM
GMDN Term
Electroencephalographic monitoring system
Device Class
Class II
Regulation Number
882.1360
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from Epi-Minder Pty, Ltd.

See all devices from Epi-Minder Pty, Ltd. →

Properties

  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No