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Smtp XDF06801

by SMTP Medical Co., Ltd.

Smtp XDF06801 is a device classified as Unclassified made by SMTP Medical Co., Ltd., listed in FDA GUDID since 24 Sep 2025 (UDI-DI 06972603515837), 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 Number06972603515837 UDI-DI Date24 Sep 2025ListedStatusListed 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  • Withdrawn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

Trade name
Smtp
Generic name
Instrument tray, reusable
Model / reference
XDF06801
Primary DI / UDI-DI
06972603515837
FDA product code
LFL
GMDN term
Instrument tray, reusable
Device class
U
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Unsafe

Similar devices

Other devices filed under FDA product code LFL (Instrument, Ultrasonic Surgical).

Other devices from SMTP Medical Co., Ltd.

See all devices from SMTP Medical Co., Ltd. →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)