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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 70° Ø 2.7MM WL 105MM rigid, TL 164mm, rod lens system FDA UDI
Model / Reference
8476435 FDA UDI
Description
TELESCOPE 70° Ø 2.7MM WL 105MM rigid, TL 164mm, rod lens system FDA UDI

Identifiers

Catalog Number
8476.435 FDA UDI
Primary DI / UDI-DI
04055207017586 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
Not 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

Dimensions & Sizes

Size
Length — 105 Millimeter FDA UDI
Angle — 70 degree FDA UDI
Outer Diameter — 2.7 Millimeter FDA UDI

The PANOVIEW PLUS HD is a high-quality, reusable rigid endoscope telescope designed for examination of body cavities following natural tracts or surgical cavities. It provides the illumination and image transmission capabilities of a rigid endoscope through the sheath of the endoscope.

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 8c4ab5e4-3244-4405-ba40-46935ba85e8f 37 fields · synced Jul 12, 2026