Identity
- Trade Name
- Laryngoscope FDA UDI
- Generic Name
- Flexible video nasopharyngoscope FDA UDI
- Device Name
- Video Nasopharyngo-laryngoscope FDA UDI
- Model / Reference
- RSX USB P FDA UDI
- Description
- Video Nasopharyngo-laryngoscope FDA UDI
Identifiers
- Catalog Number
- M205220310101 FDA UDI
- Primary DI / UDI-DI
- B809M2052203101010 FDA UDI
- 510(k) Number
- K150248 FDA UDI
- FDA Product Code
- EQN FDA UDI
- GMDN Term
- Flexible video nasopharyngoscope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.4760 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
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Laryngoscope by orlvision GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K150248 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
- orlvision GmbH
Sources (1)
- FDA UDI c4c3d625-a641-4154-a5ac-18a8e6188b1a 36 fields · synced May 30, 2026