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Plug/Ring Set

FDA UDI

Class II (US FDA UDI)

by Boston Medical Products, Inc.

Identity

Trade Name
Plug/Ring Set FDA UDI
Generic Name
Tracheostomy tube decannulation cap FDA UDI
Device Name
Size: 10 FDA UDI
Model / Reference
311006 FDA UDI
Description
Size: 10 FDA UDI

Identifiers

Catalog Number
311006 FDA UDI
Primary DI / UDI-DI
EBES3110060 FDA UDI
510(k) Number
K802916 FDA UDI
FDA Product Code
BTO FDA UDI
GMDN Term
Tracheostomy tube decannulation cap 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

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

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

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Tracheostomy tube decannulation cap

Plug/Ring Set by Boston Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tracheostomy tube decannulation cap.

Cleared under the same submission

K802916 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Medical Products, Inc.

Sources (1)

  • FDA UDI 56611193-886c-452c-a46c-f369cfa17d76 38 fields · synced Jun 9, 2026