Raw Surgical Corporation

FDA UDI

Class I (US FDA UDI)

by Raw Surgical Corporation

Identity

Trade Name: Raw Surgical Corporation FDA UDI
Generic Name: Bone cutting forceps, reusable FDA UDI
Device Name: RUSKIN BONE SPLITTING FORCEPS, Straight blades, Double-action, Overall length 71/4" (18.4cm) FDA UDI
Model / Reference: KERRISON RONGEUR FDA UDI
Description: RUSKIN BONE SPLITTING FORCEPS, Straight blades, Double-action, Overall length 71/4" (18.4cm) FDA UDI

Identifiers

Catalog Number: RSC-3228618 FDA UDI
Primary DI / UDI-DI: G508RSC32286180 FDA UDI
FDA Product Code: HTZ FDA UDI
GMDN Term: Bone cutting forceps, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone cutting forceps, reusable

Raw Surgical Corporation by Raw Surgical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Raw Surgical Corporation

Sources (1)

FDA UDI 68ebd28c-2a05-446e-bb71-a954c2a3b53a 34 fields · synced May 30, 2026