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MICROTECH SUMMIT 1200 RIC 312t

by Starkey Laboratories Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00842318117090 UDI-DI Date10 Jan 2017ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Microtech
Generic Name
Tinnitus masking application software
Model / Ref / Catalog
SUMMIT 1200 RIC 312t, 64265-S
Primary DI / UDI-DI
00842318117090
FDA Product Code
ESD, KLW
GMDN Term
Tinnitus masking application software
Device Class
Class I
Regulation Number
874.3300, 874.3400
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Starkey Laboratories Inc.

See all devices from Starkey Laboratories Inc. →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

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