← Back to catalogue

Laryseal MRI Laryngeal Mask Airway Size 2

FDA UDI

Class I (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
Laryseal MRI Laryngeal Mask Airway Size 2 FDA UDI
Generic Name
Laryngeal mask airway, single-use FDA UDI
Model / Reference
038-94-420U FDA UDI

Identifiers

Primary DI / UDI-DI
05055788733683 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

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
MRI Safety
MR Safe FDA UDI

Category: Laryngeal mask airway, single-use

Laryseal MRI Laryngeal Mask Airway Size 2 by Flexicare Medical Limited — 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

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

Manufacturer

Manufacturer
Flexicare Medical Limited

Sources (1)

  • FDA UDI e5cf9d4e-969f-428f-a9a1-3a7063818ded 32 fields · synced May 31, 2026