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Spacelabs Healthcare Tay

by Spacelabs Healthcare (Washington), Inc 31 variants

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number30841522122860 UDI-DI Date15 Feb 2018ListedStatusListed 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  • Withdrawn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
Spacelabs Healthcare
Generic Name
Electrocardiographic long-term ambulatory recording support kit
Model / Ref / Catalog
TAY, 50-0191
Primary DI / UDI-DI
30841522122860
FDA Product Code
DSH
GMDN Term
Electrocardiographic long-term ambulatory recording support kit
Device Class
Class II
Regulation Number
870.2800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrocardiographic long-term ambulatory recording support kit

Other devices from Spacelabs Healthcare (Washington), Inc

See all devices from Spacelabs Healthcare (Washington), Inc →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number

Other properties (11)

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