← Back to catalogue

Shark

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
SHARK FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI
Device Name
CUTTING ELECTRODE MONO 0° 22FR FDA UDI
Model / Reference
46792235 FDA UDI
Description
CUTTING ELECTRODE MONO 0° 22FR FDA UDI

Identifiers

Catalog Number
46792235 FDA UDI
Primary DI / UDI-DI
04055207053621 FDA UDI
FDA Product Code
FAS FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4300 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 7.33333333333 Millimeter FDA UDI
Angle — 0 degree FDA UDI

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

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 cd71b23f-91bc-4808-aba8-7966b6e96066 38 fields · synced May 30, 2026