← Back to catalogue

Panoview Plus

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
PANOVIEW PLUS FDA UDI
Generic Name
Rigid optical cystourethroscope FDA UDI
Device Name
CYSTOSCOPE 25° 14FR WL 218MM rigid, with straight ocular lens, working channel 5Fr, atraumatic distal tip, TL 358mm, rod lens system FDA UDI
Model / Reference
8642403 FDA UDI
Description
CYSTOSCOPE 25° 14FR WL 218MM rigid, with straight ocular lens, working channel 5Fr, atraumatic distal tip, TL 358mm, rod lens system FDA UDI

Identifiers

Catalog Number
8642.403 FDA UDI
Primary DI / UDI-DI
04055207018262 FDA UDI
FDA Product Code
FBO FDA UDI
GMDN Term
Rigid optical cystourethroscope 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 — 4.66666666666 Millimeter FDA UDI
Angle — 25 degree FDA UDI
Length — 218 Millimeter FDA UDI

Category: Rigid optical cystourethroscope

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 cystourethroscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI 1873b371-f6e1-480c-bad6-7bc34c62a254 37 fields · synced May 29, 2026