Identity
- Trade Name
- PANOVIEW PLUS HD FDA UDI
- Generic Name
- Rigid endoscope telescope FDA UDI
- Device Name
- DISCOSCOPE 25° Ø 5.9MM SL 122MM rigid, with lateral ocular lens, working channel Ø 3.1 mm, irrigation channel Ø 1.2 mm, TL 236 mm, rod lens system FDA UDI
- Model / Reference
- 892108253 FDA UDI
- Description
- DISCOSCOPE 25° Ø 5.9MM SL 122MM rigid, with lateral ocular lens, working channel Ø 3.1 mm, irrigation channel Ø 1.2 mm, TL 236 mm, rod lens system FDA UDI
Identifiers
- Catalog Number
- 892108253 FDA UDI
- Primary DI / UDI-DI
- 04055207035108 FDA UDI
- FDA Product Code
- HRX FDA UDI
- GMDN Term
- Rigid endoscope telescope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1100 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
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 5.9 Millimeter FDA UDILength — 122 Millimeter FDA UDIAngle — 25 degree FDA UDI
Panoview Plus Hd 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 7074a722-264b-4dcd-864f-ebd8c66b1c09 37 fields · synced Jun 8, 2026