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Volmed Brasil

FDA UDI

Class I (US FDA UDI)

by Volmed Brasil Equipamentos Ltda

Identity

Trade Name
VOLMED BRASIL FDA UDI
Generic Name
Fluid transfer set, general-purpose FDA UDI
Device Name
CF2 02-WAY IRRIGATION SET FDA UDI
Model / Reference
AEQU11 FDA UDI
Description
CF2 02-WAY IRRIGATION SET FDA UDI

Identifiers

Primary DI / UDI-DI
07908783000060 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Fluid transfer set, general-purpose FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Fluid transfer set, general-purpose

Volmed Brasil by Volmed Brasil Equipamentos Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluid transfer set, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f9b2e1a5-53e3-46ae-ae77-2dedb17c0592 33 fields · synced May 30, 2026