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Eragon Modular

FDA UDI

Class II (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
ERAGON MODULAR FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
CLAW GRASPING FORCEPS Ø 5MM BNDL 3 part, SL 330mm FDA UDI
Model / Reference
83934945 FDA UDI
Description
CLAW GRASPING FORCEPS Ø 5MM BNDL 3 part, SL 330mm FDA UDI

Identifiers

Catalog Number
83934945 FDA UDI
Primary DI / UDI-DI
04055207061251 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, 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

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 Millimeter FDA UDI

Category: Rigid endoscopic tissue manipulation forceps, reusable

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

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, 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 f61c8ab5-84dd-4af4-9b17-a4ea91a70b1d 36 fields · synced May 31, 2026