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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 - Robertazzi 28Fr Nasopharyngeal Airway, 1ea - Lubricating Jelly FDA UDI
Model / Reference
03 FDA UDI
Description
1ea - Robertazzi 28Fr Nasopharyngeal Airway, 1ea - Lubricating Jelly FDA UDI

Identifiers

Catalog Number
11-110 FDA UDI
Primary DI / UDI-DI
M68911110030 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
Not 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

Nasal Trumpet by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b02cf219-bd44-4a09-94f3-5ec2eacca4f2 36 fields · synced Jun 1, 2026