Identity
- Trade Name
- PANOVIEW PLUS FDA UDI
- Generic Name
- Rigid intubation laryngoscope, reusable FDA UDI
- Device Name
- LARYN-PHARYNGOSCOPE 90° Ø 10MM WL 161MM rigid, 2 zoom zone, TL 237mm, rod lens system, manual focus, reusable FDA UDI
- Model / Reference
- 885090 FDA UDI
- Description
- LARYN-PHARYNGOSCOPE 90° Ø 10MM WL 161MM rigid, 2 zoom zone, TL 237mm, rod lens system, manual focus, reusable FDA UDI
Identifiers
- Catalog Number
- 885090 FDA UDI
- Primary DI / UDI-DI
- 04055207055045 FDA UDI
- FDA Product Code
- CCW FDA UDI
- GMDN Term
- Rigid intubation laryngoscope, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5540 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Angle — 90 degree FDA UDILength — 161 Millimeter FDA UDIOuter Diameter — 10 Millimeter FDA UDI
Panoview Plus by Richard Wolf GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 I | Pending data |
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Manufacturer
- Manufacturer
- Richard Wolf GmbH
Sources (1)
- FDA UDI e074beb1-bf20-40e9-8bdf-8570d5954356 37 fields · synced May 30, 2026