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Usb™ Universal Stylet Bougie 15fr Od 5.0 Mm

FDA UDI

Class I (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name
USB™ UNIVERSAL STYLET BOUGIE 15FR OD 5.0 MM FDA UDI
Generic Name
Endotracheal tube introducer, single-use FDA UDI
Device Name
USB™ UNIVERSAL STYLET BOUGIE 15FR OD 5.0 MM FDA UDI
Model / Reference
8090015 FDA UDI
Description
USB™ UNIVERSAL STYLET BOUGIE 15FR OD 5.0 MM FDA UDI

Identifiers

Primary DI / UDI-DI
05030267153213 FDA UDI
FDA Product Code
BSR FDA UDI
GMDN Term
Endotracheal tube introducer, 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

Yes

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

Category: Endotracheal tube introducer, single-use

Usb™ Universal Stylet Bougie 15fr Od 5.0 Mm by Intersurgical Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endotracheal tube introducer, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fdf0902b-2b8b-4c93-9a20-ecd93fb860ca 34 fields · synced May 29, 2026