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Introes Pocket Bougie

FDA UDI

Class I (US FDA UDI)

by BOMImed Inc

Identity

Trade Name
INTROES POCKET BOUGIE FDA UDI
Generic Name
Endotracheal tube introducer, single-use FDA UDI
Device Name
INTROES POCKET BOUGIE - Endotracheal Tuber Introducer, 14FR (4.7mm) x 60cm FDA UDI
Model / Reference
OL-E12102 FDA UDI
Description
INTROES POCKET BOUGIE - Endotracheal Tuber Introducer, 14FR (4.7mm) x 60cm FDA UDI

Identifiers

Catalog Number
OL-E12102 FDA UDI
Primary DI / UDI-DI
10629160000018 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

No

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

Category: Endotracheal tube introducer, single-use

Introes Pocket Bougie by BOMImed Inc — 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

Manufacturer
BOMImed Inc

Sources (1)

  • FDA UDI e26120b1-6c97-4278-b6c9-063b132daee6 34 fields · synced May 31, 2026