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Mallinckrodt

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name
Mallinckrodt FDA UDI
Generic Name
Artificial airway stylet, single-use FDA UDI
Device Name
Intubating Stylet FDA UDI
Model / Reference
85863 FDA UDI
Description
Intubating Stylet FDA UDI

Identifiers

Primary DI / UDI-DI
80884522004076 FDA UDI
FDA Product Code
BSR FDA UDI
GMDN Term
Artificial airway stylet, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5790 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

Yes

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
Catheter Gauge — 6 French FDA UDI

Category: Artificial airway stylet, single-use

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

Similar devices

Also classified as Artificial airway stylet, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI c0a8db7c-6c7a-4291-8e02-31f71f7cb50d 35 fields · synced May 30, 2026