← Back to catalogue

Sharn Inc

FDA UDI

Class I (US FDA UDI)

by Sharn Anesthesia

Identity

Trade Name
Sharn Inc FDA UDI
Generic Name
Anaesthesia face mask, single-use FDA UDI
Device Name
FLEXIBLE DISPOS LARYNGEAL MASK, SIZE 2.5 5/PK FDA UDI
Model / Reference
LMF-327-250H FDA UDI
Description
FLEXIBLE DISPOS LARYNGEAL MASK, SIZE 2.5 5/PK FDA UDI

Identifiers

Catalog Number
LMF-327-250H FDA UDI
Primary DI / UDI-DI
00817518020259 FDA UDI
FDA Product Code
CAE FDA UDI
GMDN Term
Anaesthesia face mask, 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

Category: Anaesthesia face mask, single-use

Sharn Inc by Sharn Anesthesia — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia face mask, 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
Sharn Anesthesia

Sources (1)

  • FDA UDI 8448f32a-18a2-4422-9163-e20ea349cf2a 35 fields · synced Jun 6, 2026