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Lma Airway Management

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
LMA AIRWAY MANAGEMENT FDA UDI
Generic Name
Laryngeal mask airway, reusable FDA UDI
Device Name
LMA ProSeal™ Size 2.5 FDA UDI
Model / Reference
IPN922896 FDA UDI
Description
LMA ProSeal™ Size 2.5 FDA UDI

Identifiers

Catalog Number
150025 FDA UDI
Primary DI / UDI-DI
15060112318716 FDA UDI
FDA Product Code
CAE FDA UDI
GMDN Term
Laryngeal mask airway, reusable 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Laryngeal mask airway, reusable

Lma Airway Management by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngeal mask airway, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 8144ed40-dfbc-4102-be18-dc3d763edcca 37 fields · synced Jun 8, 2026