← Back to catalogue

Esophageal Stent

FDA UDI

Class I (US FDA UDI)

by Hood, E Benson Laboratories Inc

Identity

Trade Name
Esophageal Stent FDA UDI
Generic Name
Nasopharyngeal airway, single-use FDA UDI
Device Name
Esophageal Prosthesis FDA UDI
Model / Reference
ESS-14 FDA UDI
Description
Esophageal Prosthesis FDA UDI

Identifiers

Primary DI / UDI-DI
00815347023717 FDA UDI
FDA Product Code
KAC FDA UDI
GMDN Term
Nasopharyngeal airway, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Nasopharyngeal airway, single-use

Esophageal Stent by Hood, E Benson Laboratories Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasopharyngeal airway, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 9d062147-8ed7-4b07-aab7-9b0515817309 33 fields · synced Jun 1, 2026