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Unifusor

by Statcorp Medical 4 variants

Unifusor (803FGA) is a Class I device made by Statcorp Medical, listed in FDA GUDID since 20 Aug 2019 (UDI-DI 10841522127458), registry data as of 8 Jun 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 8 Jun 2026.

Regulatory status

as of registry sync 8 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10841522127458 UDI-DI Date20 Aug 2019ListedStatusListed 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  • Withdrawn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

Generic name
Intravenous pressure infusor, manual, reusable
Model / Ref / Catalog
Unifusor, 803FGA
Primary DI / UDI-DI
10841522127458
FDA product code
KZD
GMDN term
Intravenous pressure infusor, manual, reusable
Device class
Class I
Regulation number
880.5420
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KZD (INFUSOR, PRESSURE, FOR I.V. BAGS).

Other devices from Statcorp Medical

See all devices from Statcorp Medical →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)