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Mallinckrodt

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Mallinckrodt FDA UDI
Generic Name
Basic endotracheal tube, single-use FDA UDI
Device Name
Oral/Nasal Tracheal Tube Cuffless FDA UDI
Model / Reference
86466 FDA UDI
Description
Oral/Nasal Tracheal Tube Cuffless FDA UDI

Identifiers

Catalog Number
86466 FDA UDI
Primary DI / UDI-DI
60884522005505 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
Not 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

No

FDA UDI

Mallinckrodt by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI e7cfdde7-6eab-443b-8fbd-3365e55027ce 38 fields · synced Jun 8, 2026