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Angled Stem T-Tube

FDA UDI

Class II (US FDA UDI)

by Hood, E Benson Laboratories Inc

Identity

Trade Name
Angled Stem T-Tube FDA UDI
Generic Name
Tracheostomy tube, non-reinforced, non-customized, single-use FDA UDI
Device Name
Montgomery Tracheal T-Tube FDA UDI
Model / Reference
AST-12-S FDA UDI
Description
Montgomery Tracheal T-Tube FDA UDI

Identifiers

Primary DI / UDI-DI
00815347020297 FDA UDI
510(k) Number
K873742 FDA UDI
FDA Product Code
BTO FDA UDI
GMDN Term
Tracheostomy tube, non-reinforced, non-customized, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5800 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Tracheostomy tube, non-reinforced, non-customized, single-use

Angled Stem T-Tube by Hood, E Benson Laboratories Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tracheostomy tube, non-reinforced, non-customized, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a35a2ebe-ec38-4977-87ac-6c81d6d9b459 34 fields · synced Jun 1, 2026