Identity
- Trade Name
- PANOVIEW FDA UDI
- Generic Name
- Optical proctoscope, reusable FDA UDI
- Device Name
- TELESCOPE 40° Ø 6.6MM SL 321MM FDA UDI
- Model / Reference
- 8840402 FDA UDI
- Description
- TELESCOPE 40° Ø 6.6MM SL 321MM FDA UDI
Identifiers
- Catalog Number
- 8840.402 FDA UDI
- Primary DI / UDI-DI
- 04055207020937 FDA UDI
- FDA Product Code
- GCM FDA UDI
- GMDN Term
- Optical proctoscope, reusable 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
- Angle — 40 degree FDA UDIOuter Diameter — 6.6 Millimeter FDA UDILength — 321 Millimeter FDA UDI
Panoview 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 a3846c9d-9f84-44a3-afca-967851e79459 37 fields · synced May 30, 2026