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Laryngeal Mask Tube

FDA UDI

Class I (US FDA UDI)

by Fortune Medical Instrument Corp.

Identity

Trade Name
Laryngeal Mask Tube FDA UDI
Generic Name
Laryngeal mask airway, reusable FDA UDI
Model / Reference
1580-0010 FDA UDI

Identifiers

Primary DI / UDI-DI
14711182603097 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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, reusable

Laryngeal Mask Tube by Fortune Medical Instrument Corp. — 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

Sources (1)

  • FDA UDI 377730a1-274a-4161-9c07-151e5c66652a 32 fields · synced May 30, 2026