Identity
- Trade Name
- AEROBIKA OPEP Manometer FDA UDI
- Generic Name
- Positive pressure airway secretion-clearing device FDA UDI
- Device Name
- AEROBIKA OPEP Manometer FDA UDI
- Model / Reference
- 110502 FDA UDI
- Description
- AEROBIKA OPEP Manometer FDA UDI
Identifiers
- Catalog Number
- 11050294025 FDA UDI
- Primary DI / UDI-DI
- 62860110502029 FDA UDI
- 510(k) Number
- K150173 FDA UDI
- FDA Product Code
- BWF FDA UDI
- GMDN Term
- Positive pressure airway secretion-clearing device FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5690 FDA UDI
- Commercial Distribution
- Not 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
AEROBIKA OPEP Manometer by Trudell Medical International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K150173 also covers:
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
- Trudell Medical International
Sources (1)
- FDA UDI 484d061d-d549-4364-a29c-9fdf3bc10c49 37 fields · synced May 30, 2026