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Sheridan

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
SHERIDAN FDA UDI
Generic Name
Artificial airway stylet, single-use FDA UDI
Device Name
STYLET,SOFT TIP,6 FR FDA UDI
Model / Reference
IPN926924 FDA UDI
Description
STYLET,SOFT TIP,6 FR FDA UDI

Identifiers

Catalog Number
5-15120 FDA UDI
Primary DI / UDI-DI
14026704760067 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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Artificial airway stylet, single-use

Sheridan by Teleflex Incorporated — 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
Teleflex Incorporated

Sources (1)

  • FDA UDI a9d3ca6f-5b7a-4b57-addb-901e0b026f57 35 fields · synced Jun 8, 2026