← Back to catalogue

Panoview

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
PANOVIEW FDA UDI
Generic Name
Rigid endoscope telescope FDA UDI
Device Name
TELESCOPE 30° Ø 2.4MM SL 80MM rigid, TL 137mm, rod lens system FDA UDI
Model / Reference
8871412 FDA UDI
Description
TELESCOPE 30° Ø 2.4MM SL 80MM rigid, TL 137mm, rod lens system FDA UDI

Identifiers

Catalog Number
8871.412 FDA UDI
Primary DI / UDI-DI
04055207021415 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Rigid endoscope telescope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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 — 2.4 Millimeter FDA UDI
Length — 80 Millimeter FDA UDI

Category: Rigid endoscope telescope

Panoview 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

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

Manufacturer

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI 21ac450c-9f94-48b7-878f-05ed3943ca85 36 fields · synced Jun 8, 2026