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Pico 66002005

by Smith & Nephew Medical, Ltd.

Pico 66002005 is a Class II device made by Smith & Nephew Medical, Ltd., listed in FDA GUDID since 27 Nov 2018 (UDI-DI 05000223493950), 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 Number05000223493950 UDI-DI Date27 Nov 2018ListedStatusListed 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  • Withdrawn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
Pico
Generic name
Negative-pressure wound therapy system, electric, single-use
Model / Ref / Catalog
66002005
Primary DI / UDI-DI
05000223493950
FDA product code
OMP, QFC
GMDN term
Negative-pressure wound therapy system, electric, single-use
Device class
Class II
Regulation number
878.4780, 878.4783
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Size
Length — 5.9000 Inch
Width — 5.9000 Inch
Width — 15 Centimeter
Length — 15 Centimeter

Related devices

Category: Negative-pressure wound therapy system, electric, single-use

Similar devices in this category

Other devices filed under Negative-pressure wound therapy system, electric, single-use.

Other devices from Smith & Nephew Medical, Ltd.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)