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Eragon Bipolar

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
ERAGON BIPOLAR FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Device Name
GRASPING FORCEPS BIPO Ø 5.5MM BNDL 3 part, SL 435mm FDA UDI
Model / Reference
839400342 FDA UDI
Description
GRASPING FORCEPS BIPO Ø 5.5MM BNDL 3 part, SL 435mm FDA UDI

Identifiers

Catalog Number
839400342 FDA UDI
Primary DI / UDI-DI
04055207061091 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

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 — 5.5 Millimeter FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

Eragon Bipolar 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, bipolar, 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 fd504fa0-f772-4dc4-9815-af833f09fd1a 36 fields · synced Jun 1, 2026