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LIVVE™ Size 4.5

FDA UDI

Class I (US FDA UDI)

by Wm&Dg

Identity

Trade Name
LIVVE™ Size 4.5 FDA UDI
Generic Name
Laryngeal mask airway, single-use FDA UDI
Device Name
The LIVVE™ (Laryngeal, Intubating, Visualizing, Ventilating, and Extubating Device) is a single-use, non-sterile, 2-lumen channel device with a cushioned cuff to ensure a semi-closed ventilation system is maintained during ventilation and oral intubation. Adult size 4.5: > 90 kg (198 lbs) FDA UDI
Model / Reference
LB1545 FDA UDI
Description
The LIVVE™ (Laryngeal, Intubating, Visualizing, Ventilating, and Extubating Device) is a single-use, non-sterile, 2-lumen channel device with a cushioned cuff to ensure a semi-closed ventilation system is maintained during ventilation and oral intubation. Adult size 4.5: > 90 kg (198 lbs) FDA UDI

Identifiers

Catalog Number
LB1545 FDA UDI
Primary DI / UDI-DI
00850027063034 FDA UDI
FDA Product Code
CAE FDA UDI
GMDN Term
Laryngeal mask airway, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5110 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Category: Laryngeal mask airway, single-use

LIVVE™ Size 4.5 by Wm&Dg — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngeal mask airway, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wm&Dg

Sources (1)

  • FDA UDI c05c2c12-0b7d-4105-b46f-50a2ccea182f 34 fields · synced May 30, 2026