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Volmed Brasil AEQU11

by Volmed Brasil Equipamentos Ltda

Volmed Brasil AEQU11 is a Class I device made by Volmed Brasil Equipamentos Ltda, listed in FDA GUDID since 6 Mar 2025 (UDI-DI 07908783000060), 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 Number07908783000060 UDI-DI Date6 Mar 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  • Withdrawn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
Volmed Brasil
Generic name
Fluid transfer set, general-purpose
Model / reference
AEQU11
Primary DI / UDI-DI
07908783000060
FDA product code
NBH
GMDN term
Fluid transfer set, general-purpose
Device class
Class I
Regulation number
888.1100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Fluid transfer set, general-purpose

Similar devices in this category

Other devices filed under Fluid transfer set, general-purpose.

Other devices from Volmed Brasil Equipamentos Ltda

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Properties

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