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APOTECA APOTECAped

by Aea SRL

APOTECA APOTECAped is a Class II device made by Aea SRL, listed in FDA GUDID since 22 May 2018 (UDI-DI 05060304050243), 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 Number05060304050243 UDI-DI Date22 May 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  • Withdrawn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
Apoteca
Generic name
Pharmaceutical fluid-dispensing system
Model / reference
APOTECAped
Primary DI / UDI-DI
05060304050243
FDA product code
NEP
GMDN term
Pharmaceutical fluid-dispensing system
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pharmaceutical fluid-dispensing system

Other devices from Aea SRL

See all devices from Aea SRL →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)