← Back to catalogue

Armstrong

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
Armstrong FDA UDI
Generic Name
Tympanostomy tube FDA UDI
Device Name
VENT TUBE 1010171 50PK ARMSTRNG BEV GROM FDA UDI
Model / Reference
1010171 FDA UDI
Description
VENT TUBE 1010171 50PK ARMSTRNG BEV GROM FDA UDI

Identifiers

Primary DI / UDI-DI
00763000038540 FDA UDI
510(k) Number
K151067 FDA UDI
FDA Product Code
ETD FDA UDI
GMDN Term
Tympanostomy tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3880 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 1.14 Millimeter FDA UDI

Category: Tympanostomy tube

Armstrong by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tympanostomy tube.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c0446a4f-6f8e-4d21-9171-31139c03f9d4 36 fields · synced Jun 8, 2026