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Traditonal Guedel Airway, Orange, 110mm

FDA UDIEUDAMED

Class I (US FDA UDI)

by Besmed Health Business Corp.

Identity

Trade Name
TRADITONAL GUEDEL AIRWAY,ORANGE,110MM FDA UDI
Generic Name
Oropharyngeal airway, single-use FDA UDI
Device Name
TRADITONAL GUEDEL AIRWAY,ORANGE,110MM FDA UDI
Model / Reference
AW-61311 FDA UDI
Description
TRADITONAL GUEDEL AIRWAY,ORANGE,110MM FDA UDI

Identifiers

Primary DI / UDI-DI
04716770613116 FDA UDI
FDA Product Code
CAE FDA UDI
GMDN Term
Oropharyngeal airway, 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

Yes

FDA UDI

Category: Oropharyngeal airway, single-use

Traditonal Guedel Airway, Orange, 110mm by Besmed Health Business Corp. — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Oropharyngeal airway, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI b5c88dd8-59c3-4e4a-9553-f7d80cb195e5 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 4, 2026