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Sonicision 7 SCD7A48

by Covidien LP

Sonicision 7 SCD7A48 is a device classified as Unclassified made by Covidien LP, listed in FDA GUDID since 25 Apr 2022 (UDI-DI 10884521794801), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10884521794801 UDI-DI Date25 Apr 2022ListedStatusListed 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  • Withdrawn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
Sonicision 7
Generic name
Soft-tissue ultrasonic surgical system
Model / reference
SCD7A48
Primary DI / UDI-DI
10884521794801
FDA product code
LFL
GMDN term
Soft-tissue ultrasonic surgical system
Device class
U
GUDID distribution status
In Commercial Distribution
Size
Length — 48 Centimeter

Related devices

Category: Soft-tissue ultrasonic surgical system

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Properties

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