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Technical Products

FDA UDI

Class I (US FDA UDI)

by Technical Products, Inc.

Identity

Trade Name
Technical Products FDA UDI
Generic Name
Tracheostomy tube, non-reinforced, non-customized, reusable FDA UDI
Device Name
TRACHEAL CANNULA FDA UDI
Model / Reference
TC-1113T FDA UDI
Description
TRACHEAL CANNULA FDA UDI

Identifiers

Catalog Number
TC-1113T FDA UDI
Primary DI / UDI-DI
B051TC1113 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Tracheostomy tube, non-reinforced, non-customized, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tracheostomy tube, non-reinforced, non-customized, reusable

Technical Products by Technical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tracheostomy tube, non-reinforced, non-customized, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Technical Products, Inc.

Sources (1)

  • FDA UDI 7488d7b1-b572-4cf4-bde7-1690c476af8b 34 fields · synced May 30, 2026