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IVD Rongeur

FDA UDI

Class I (US FDA UDI)

by Koros USA, Inc.

Identity

Trade Name
IVD Rongeur FDA UDI
Generic Name
Craniofacial rongeur, reusable FDA UDI
Device Name
Intervertebral Disk Rongeur Straight 2mm 9" FDA UDI
Model / Reference
7379-20 FDA UDI
Description
Intervertebral Disk Rongeur Straight 2mm 9" FDA UDI

Identifiers

Catalog Number
7379-20 FDA UDI
Primary DI / UDI-DI
10840199520074 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Craniofacial rongeur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal rongeurOrthopaedic joint/limb rongeurCraniofacial rongeur, reusableRib rongeur

IVD Rongeur by Koros USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rib rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Koros USA, Inc.

Sources (1)

  • FDA UDI aced4203-ac06-4052-a001-b2e23bd9f17a 37 fields · synced May 30, 2026