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Panoview

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
PANOVIEW FDA UDI
Generic Name
Rigid optical laparoscope FDA UDI
Device Name
OP-ENDOSCOPE 0° Ø 5.5MM SL 215MM rigid, with lateral ocular lens, working channel Ø 3.5mm, TL 370mm, rod lens system FDA UDI
Model / Reference
8920401 FDA UDI
Description
OP-ENDOSCOPE 0° Ø 5.5MM SL 215MM rigid, with lateral ocular lens, working channel Ø 3.5mm, TL 370mm, rod lens system FDA UDI

Identifiers

Catalog Number
8920.401 FDA UDI
Primary DI / UDI-DI
04055207022092 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid optical laparoscope 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
Angle — 0 degree FDA UDI
Length — 215 Millimeter FDA UDI
Outer Diameter — 5.5 Millimeter FDA UDI

Category: Rigid optical laparoscope

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

Similar devices

Also classified as Rigid optical laparoscope.

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 75cb08d8-3ad0-48c3-99a3-aa81ef35ec8d 36 fields · synced May 30, 2026