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Panoview Plus Hd

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
PANOVIEW PLUS HD FDA UDI
Generic Name
Rigid endoscope telescope FDA UDI
Device Name
TELESCOPE 30° Ø 2.7MM WL 103MM rigid, TL 161mm, rod lens system FDA UDI
Model / Reference
8476433 FDA UDI
Description
TELESCOPE 30° Ø 2.7MM WL 103MM rigid, TL 161mm, rod lens system FDA UDI

Identifiers

Catalog Number
8476.433 FDA UDI
Primary DI / UDI-DI
04055207017579 FDA UDI
FDA Product Code
GCM 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
Angle — 30 degree FDA UDI
Outer Diameter — 2.7 Millimeter FDA UDI
Length — 103 Millimeter FDA UDI

Category: Rigid endoscope telescope

Panoview Plus Hd 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 f646f3cc-70f3-4933-afbf-a90f822586b1 36 fields · synced May 30, 2026