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MN3300

by Medi Nuclear Corp., Inc.

MN3300 is a device of GMDN type earplugs (FDA Class II; FDA product code IYT, System, Rebreathing, Radionuclide) made by Medi Nuclear Corp., Inc., listed in FDA GUDID since 9 Jun 2017 (UDI-DI 00857863007611), 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 Number00857863007611 UDI-DI Date9 Jun 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  • Withdrawn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

Generic name
Earplugs, single-use
Model / reference
MN3300
Primary DI / UDI-DI
00857863007611
FDA product code
IYT
GMDN term
Earplugs, single-use
Device class
Class II
Regulation number
892.1390
GUDID distribution status
In Commercial Distribution

Related devices

Category: Earplugs, single-use

Similar devices

Other devices filed under FDA product code IYT (System, Rebreathing, Radionuclide).

Other devices from Medi Nuclear Corp., Inc.

See all devices from Medi Nuclear Corp., Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)