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Panoview Plus

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
PANOVIEW PLUS FDA UDI
Generic Name
Rigid optical nephroscope FDA UDI
Device Name
NEPHROSCOPE 20° 24FR WL 224MM rigid, with parallel ocular lens, working channel for instruments up to 10.5Fr, TL 387mm, rod lens system FDA UDI
Model / Reference
8965401 FDA UDI
Description
NEPHROSCOPE 20° 24FR WL 224MM rigid, with parallel ocular lens, working channel for instruments up to 10.5Fr, TL 387mm, rod lens system FDA UDI

Identifiers

Catalog Number
8965.401 FDA UDI
Primary DI / UDI-DI
04055207023310 FDA UDI
FDA Product Code
FGA FDA UDI
GMDN Term
Rigid optical nephroscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 8 Millimeter FDA UDI
Angle — 20 degree FDA UDI
Length — 224 Millimeter FDA UDI

Category: Rigid optical nephroscope

Panoview Plus by Richard Wolf GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical nephroscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI fad72558-bdc0-4630-97e6-3831a24dab5e 36 fields · synced Jun 8, 2026