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Nasal Trumpet

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
Nasal Trumpet FDA UDI
Generic Name
Laryngeal mask airway, single-use FDA UDI
Device Name
1ea - sterile, pre-lubricated nasopharyngeal airway FDA UDI
Model / Reference
02 FDA UDI
Description
1ea - sterile, pre-lubricated nasopharyngeal airway FDA UDI

Identifiers

Catalog Number
11-128 FDA UDI
Primary DI / UDI-DI
M68911128020 FDA UDI
FDA Product Code
BTQ FDA UDI
GMDN Term
Laryngeal mask airway, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5100 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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: Laryngeal mask airway, single-use

Nasal Trumpet by Safeguard Us Operating, Llc — 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

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Manufacturer

Sources (1)

  • FDA UDI b45f6a8f-01b4-43ef-a533-0f14ed488265 36 fields · synced Jun 8, 2026