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Eragon Modular Mini

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
ERAGON MODULAR MINI FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
Device Name
HOOK SCISSORS INSERT Ø 3.5MM jaw length 8mm, for SL 330mm, single action, reusable FDA UDI
Model / Reference
8391227 FDA UDI
Description
HOOK SCISSORS INSERT Ø 3.5MM jaw length 8mm, for SL 330mm, single action, reusable FDA UDI

Identifiers

Catalog Number
8391227 FDA UDI
Primary DI / UDI-DI
04055207042274 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 3.5 Millimeter FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, monopolar, reusable

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

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, monopolar, reusable.

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 15cf58f9-5f15-42c7-8d62-56583286677a 36 fields · synced May 31, 2026