Identity
- Trade Name
- PANOVIEW PLUS FDA UDI
- Generic Name
- Rigid endoscope telescope FDA UDI
- Device Name
- TELESCOPE 0° Ø 2.2/2.7MM WL 482MM rigid, with straight ocular lens, TL 565mm, rod lens system FDA UDI
- Model / Reference
- 8720401 FDA UDI
- Description
- TELESCOPE 0° Ø 2.2/2.7MM WL 482MM rigid, with straight ocular lens, TL 565mm, rod lens system FDA UDI
Identifiers
- Catalog Number
- 8720.401 FDA UDI
- Primary DI / UDI-DI
- 04055207020197 FDA UDI
- FDA Product Code
- GCM FDA UDI
- GMDN Term
- Rigid endoscope telescope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 482 Millimeter FDA UDIAngle — 0 degree FDA UDI
Panoview Plus by Richard Wolf GmbH — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Richard Wolf GmbH
Sources (1)
- FDA UDI de3a1d48-f758-442c-af3e-56eb8344ee43 37 fields · synced May 30, 2026