Identity
- Trade Name
- Armstrong Activent® FDA UDI
- Generic Name
- Tympanostomy tube FDA UDI
- Device Name
- VENT TUBE 1030030 5PK ARMSTR BEV GROMMET FDA UDI
- Model / Reference
- 1030030 FDA UDI
- Description
- VENT TUBE 1030030 5PK ARMSTR BEV GROMMET FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00681490030298 FDA UDI
- 510(k) Number
- K961873 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
MR Conditional FDA UDI
Category: Tympanostomy tube
Armstrong Activent® by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Tympanostomy tube.
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- NeoZoline — JEDMED Instrument Company · Class II
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- Gyrus ACMI — Gyrus Acmi, Inc. · Class II
- TINY TRIUNE VENT TUBE — Grace Medical, Inc. · Class II
Cleared under the same submission
K961873 also covers:
- Activent® — MEDTRONIC XOMED, INC.
- Armstrong V Activent® — MEDTRONIC XOMED, INC.
- Baxter Activent® — MEDTRONIC XOMED, INC.
- Moretz Activent® — MEDTRONIC XOMED, INC.
- Pope Activent® — MEDTRONIC XOMED, INC.
- Reuter Activent® — MEDTRONIC XOMED, INC.
- Reuter Activent® — MEDTRONIC XOMED, INC.
- Shah Type Activent® — MEDTRONIC XOMED, INC.
- Sheehy Type Activent® — MEDTRONIC XOMED, INC.
- Shepard Activent® — MEDTRONIC XOMED, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Medtronic Xomed, Inc.
Sources (1)
- FDA UDI f954b2e6-315f-45a5-b940-545cf627dc67 36 fields · synced May 30, 2026