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Avanos

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
AVANOS FDA UDI
Generic Name
Basic endotracheal tube, single-use FDA UDI
Device Name
MICROCUFF* Pediatric Endotracheal Tube, Oral/Nasal Magill FDA UDI
Model / Reference
35111 FDA UDI
Description
MICROCUFF* Pediatric Endotracheal Tube, Oral/Nasal Magill FDA UDI

Identifiers

Catalog Number
35111 FDA UDI
Primary DI / UDI-DI
00609038351117 FDA UDI
510(k) Number
K080821 FDA UDI
FDA Product Code
BTR FDA UDI
GMDN Term
Basic endotracheal tube, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5730 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 4.3 Millimeter FDA UDI

Category: Basic endotracheal tube, single-use

Avanos by Avanos Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic endotracheal tube, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 21c56492-b447-45e0-b441-f2b2e84b1ba3 37 fields · synced Jun 9, 2026