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Nasopharyngeal Airway 30FR

FDA UDI

by Safeguard Us Operating, Llc

Identity

Trade Name
Nasopharyngeal Airway 30FR FDA UDI
Generic Name
Laryngeal mask airway, single-use FDA UDI
Device Name
HHNPA30-NS-EA H&H Nasopharyngeal L01-0022 x 4 white, blank label P31-207Zip Bag, 12x12 f/ CR FDA UDI
Model / Reference
1 FDA UDI
Description
HHNPA30-NS-EA H&H Nasopharyngeal L01-0022 x 4 white, blank label P31-207Zip Bag, 12x12 f/ CR FDA UDI

Identifiers

Catalog Number
HHNPA30-CA FDA UDI
Primary DI / UDI-DI
M689HHNPA30CA0105 FDA UDI
GMDN Term
Laryngeal mask airway, single-use FDA UDI

Classification

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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Laryngeal mask airway, single-use

Nasopharyngeal Airway 30FR by Safeguard Us Operating, Llc — 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 1db5d0c2-a0c1-402f-8661-89e91a2a1eee 35 fields · synced Jun 8, 2026