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Moore Tube Low-Profile Inner Cannula

FDA UDI

Class II (US FDA UDI)

by Boston Medical Products, Inc.

Identity

Trade Name
Moore Tube Low-Profile Inner Cannula FDA UDI
Generic Name
Tracheostomy tube cannula, reusable FDA UDI
Device Name
Size: 10; Type: Radiopaque FDA UDI
Model / Reference
MTT-010-LP FDA UDI
Description
Size: 10; Type: Radiopaque FDA UDI

Identifiers

Catalog Number
MTT-010-LP FDA UDI
Primary DI / UDI-DI
EBESMTT010LP0 FDA UDI
510(k) Number
K962240 FDA UDI
FDA Product Code
BTO FDA UDI
GMDN Term
Tracheostomy tube cannula, reusable 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

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Tracheostomy tube cannula, reusable

Moore Tube Low-Profile Inner Cannula by Boston Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tracheostomy tube cannula, reusable.

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 e446b913-4571-4063-bec6-ecf3f588cb53 38 fields · synced Jun 9, 2026