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Stradis Medical, LLC. HCT2057

by Stradis Medical, LLC

Listed FDA GUDID listing, not in commercial distribution

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 NumberM752HCT20570 UDI-DI Date7 Dec 2017ListedStatusListed GUDID: not 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  • Withdrawn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
Stradis Medical, LLC.
Generic Name
Cytotoxic material spill kit
Model / Reference
HCT2057
Primary DI / UDI-DI
M752HCT20570
FDA Product Code
PWT
GMDN Term
Cytotoxic material spill kit
Device Class
Class I
Regulation Number
880.6250
GUDID distribution status
Not in Commercial Distribution

Other devices from Stradis Medical, LLC

See all devices from Stradis Medical, LLC →

Properties

  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number

Other properties (10)

  • Sterile: 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
  • Manufacturing Date: No