Identity
- Trade Name
- Reuter FDA UDI
- Generic Name
- Tympanostomy tube FDA UDI
- Device Name
- VENT TUBE 14051 5PK REUTER BOB FLNG 1.27 FDA UDI
- Model / Reference
- 14051 FDA UDI
- Description
- VENT TUBE 14051 5PK REUTER BOB FLNG 1.27 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00681490039949 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
- Not 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
Reuter by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K151067 also covers:
- Armstrong — MEDTRONIC XOMED, INC.
- Armstrong — MEDTRONIC XOMED, INC.
- Armstrong — MEDTRONIC XOMED, INC.
- Baxter — MEDTRONIC XOMED, INC.
- Baxter — MEDTRONIC XOMED, INC.
- C-Flex® — MEDTRONIC XOMED, INC.
- C-Flex® — MEDTRONIC XOMED, INC.
- Donaldson — MEDTRONIC XOMED, INC.
- Donaldson — MEDTRONIC XOMED, INC.
- Donaldson — MEDTRONIC XOMED, INC.
- Goode — MEDTRONIC XOMED, INC.
- Goode — 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 5978ce07-088e-48bc-8c6d-7ffa9308e950 37 fields · synced Jun 1, 2026