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DA Anterior Rongeur

FDA UDI

Class I (US FDA UDI)

by Koros USA, Inc.

Identity

Trade Name
DA Anterior Rongeur FDA UDI
Generic Name
Bone cutter FDA UDI
Device Name
DA Anterior Long Straight Rongeur 8mm FDA UDI
Model / Reference
7353-08 FDA UDI
Description
DA Anterior Long Straight Rongeur 8mm FDA UDI

Identifiers

Catalog Number
7353-08 FDA UDI
Primary DI / UDI-DI
10840199517753 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Bone cutter 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: Bone cutter

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

Similar devices

Also classified as Bone cutter.

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 3d44bca3-736a-4aaf-9a8a-551c26dcd5e6 37 fields · synced May 30, 2026