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ET Tape

FDA UDI

Class I (US FDA UDI)

by B & B Medical Technologies, Inc.

Identity

Trade Name
ET Tape FDA UDI
Generic Name
Endotracheal tube holder FDA UDI
Device Name
Long Term Endotracheal Tube Holders, 50 units FDA UDI
Model / Reference
11025 FDA UDI
Description
Long Term Endotracheal Tube Holders, 50 units FDA UDI

Identifiers

Catalog Number
11025 FDA UDI
Primary DI / UDI-DI
00850008733147 FDA UDI
FDA Product Code
CBH FDA UDI
GMDN Term
Endotracheal tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5770 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Category: Endotracheal tube holder

ET Tape by B & B Medical Technologies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endotracheal tube holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI adf7eb3a-4ebd-4fa4-b5ce-b16816a6a284 34 fields · synced Jun 1, 2026