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Smtp XDF02801520

by SMTP Medical Co., Ltd.

Smtp XDF02801520 is a Class II device made by SMTP Medical Co., Ltd., listed in FDA GUDID since 3 Nov 2025 (UDI-DI 06972603515769), 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 Number06972603515769 UDI-DI Date3 Nov 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  • Withdrawn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
Hard-tissue ultrasonic surgical system handpiece tip
Model / reference
XDF02801520
Primary DI / UDI-DI
06972603515769
FDA product code
JDX
GMDN term
Hard-tissue ultrasonic surgical system handpiece tip
Device class
Class II
Regulation number
888.4580
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Similar devices

Other devices filed under FDA product code JDX (Instrument, Surgical, Sonic And Accessory/Attachment).

Other devices from SMTP Medical Co., Ltd.

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

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)