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MIVI High Flow Tubing

FDA UDI

Class II (US FDA UDI)

by Mivi Neurovascular

Identity

Trade Name
MIVI High Flow Tubing FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Device Name
MIVI High Flow Tubing is to be used with an external source of vacuum to aspirate, remove, or sample body fluids. FDA UDI
Model / Reference
HFT110 FDA UDI
Description
MIVI High Flow Tubing is to be used with an external source of vacuum to aspirate, remove, or sample body fluids. FDA UDI

Identifiers

Primary DI / UDI-DI
B293HFT1100 FDA UDI
FDA Product Code
BYY FDA UDI
GMDN Term
Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

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

No

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 0.11 Inch FDA UDI
Length — 112 Inch FDA UDI

Category: Suction/irrigation tubing, single-use

MIVI High Flow Tubing by Mivi Neurovascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mivi Neurovascular

Sources (1)

  • FDA UDI c147efa2-586d-496b-91db-e810954c98a2 34 fields · synced May 30, 2026