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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 endoscope telescope FDA UDI
Device Name
TELESCOPE 30° Ø 3.5MM WL 180MM rigid, TL 233mm, rod lens system FDA UDI
Model / Reference
8930462 FDA UDI
Description
TELESCOPE 30° Ø 3.5MM WL 180MM rigid, TL 233mm, rod lens system FDA UDI

Identifiers

Catalog Number
8930.462 FDA UDI
Primary DI / UDI-DI
04055207022702 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid endoscope telescope 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
Length — 180 Millimeter FDA UDI
Angle — 30 degree FDA UDI
Outer Diameter — 3.5 Millimeter FDA UDI

Category: Rigid endoscope telescope

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

Similar devices

Also classified as Rigid endoscope telescope.

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 48e02efa-5eb3-4360-ab5e-689a4f7dba9d 36 fields · synced May 30, 2026