← Back to catalogue

LSU w/Bemis Canister

FDA UDI

Class II (US FDA UDI)

by Laerdal Medical Corp.

Identity

Trade Name
LSU w/Bemis Canister FDA UDI
Generic Name
Emergency airway clearance suction system, electric FDA UDI
Device Name
The LSU is a portable, electrically powered, medical suction equipment intended for field and transport use. It is intended for intermittent operation to remove secretions, blood or vomit from a patient´s airway to allow ventilation. Higher vacuum levels are generally selected for oropharyngeal suctioning, and lower vacuum levels are usually selected for tracheal suctioning and the suctioning of children and infants. FDA UDI
Model / Reference
78002001 FDA UDI
Description
The LSU is a portable, electrically powered, medical suction equipment intended for field and transport use. It is intended for intermittent operation to remove secretions, blood or vomit from a patient´s airway to allow ventilation. Higher vacuum levels are generally selected for oropharyngeal suctioning, and lower vacuum levels are usually selected for tracheal suctioning and the suctioning of children and infants. FDA UDI

Identifiers

Catalog Number
78002001 FDA UDI
Primary DI / UDI-DI
07045430042230 FDA UDI
FDA Product Code
BTA FDA UDI
GMDN Term
Emergency airway clearance suction system, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Emergency airway clearance suction system, electric

LSU w/Bemis Canister by Laerdal Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Emergency airway clearance suction system, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Laerdal Medical Corp.

Sources (1)

  • FDA UDI 79c02f44-8329-4489-85e8-074148229587 36 fields · synced Jun 6, 2026