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TekTone Sound & Signal Mfg., Inc. SF521UL

by Tektone Sound and Signal, Mfg., 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 Number00812664023871 UDI-DI Date31 Aug 2026ListedStatusListed 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  • Withdrawn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
TekTone Sound & Signal Mfg., Inc.
Generic Name
Nurse call system
Model / Reference
SF521UL
Primary DI / UDI-DI
00812664023871
FDA Product Code
IQA
GMDN Term
Nurse call system
Device Class
Class II
Regulation Number
890.3725
GUDID distribution status
In Commercial Distribution

Other devices from Tektone Sound and Signal, Mfg., Inc.

See all devices from Tektone Sound and Signal, Mfg., Inc. →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Expiration Date: No
  • Manufacturing Date: No