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Aztec

FDA UDI

Class I (US FDA UDI)

by Aztecmed/Ent LLC

Identity

Trade Name
Aztec FDA UDI
Generic Name
ENT elevator FDA UDI
Device Name
Cottle Septum Elevator FDA UDI
Model / Reference
10-14438 FDA UDI
Description
Cottle Septum Elevator FDA UDI

Identifiers

Catalog Number
10-14438 FDA UDI
Primary DI / UDI-DI
B87110144380 FDA UDI
FDA Product Code
GEG FDA UDI
GMDN Term
ENT elevator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: ENT elevator

Aztec by Aztecmed/Ent LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT elevator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aztecmed/Ent LLC

Sources (1)

  • FDA UDI 9770e5e4-e7e2-4dea-8b43-7eef21129a05 34 fields · synced Jun 6, 2026