Identity
- Trade Name
- Olympus FDA UDI
- Generic Name
- Rigid optical rhinoscope FDA UDI
- Device Name
- Handle, for sinuscope FDA UDI
- Model / Reference
- WA96208A FDA UDI
- Description
- Handle, for sinuscope FDA UDI
Identifiers
- Catalog Number
- WA96208A FDA UDI
- Primary DI / UDI-DI
- 04042761070096 FDA UDI
- 510(k) Number
- K944072 FDA UDI
- FDA Product Code
- EOB FDA UDI
- GMDN Term
- Rigid optical rhinoscope 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
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
Moist Heat or Steam Sterilization FDA UDI
Olympus by Olympus Winter & Ibe GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K944072 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
- Olympus Winter & Ibe GmbH
Sources (1)
- FDA UDI 4d3ecbb0-f9f4-4432-934b-ecd689c15930 37 fields · synced Jun 6, 2026