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MedSource ET Tube, 9.5mm, Cuffed

FDA UDI

Class II (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource ET Tube, 9.5mm, Cuffed FDA UDI
Generic Name
Basic endotracheal tube, single-use FDA UDI
Device Name
ET Tube, 9.5mm, Cuffed FDA UDI
Model / Reference
MS-23295 FDA UDI
Description
ET Tube, 9.5mm, Cuffed FDA UDI

Identifiers

Primary DI / UDI-DI
00816703020210 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

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
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Basic endotracheal tube, single-use

MedSource ET Tube, 9.5mm, Cuffed by Medsource International Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic endotracheal tube, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 12fb4a16-45a6-46d6-bdd2-2213d5a64835 33 fields · synced May 31, 2026