Integra® Ruggles®-Redmond™

FDA UDI

Class I (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name: Integra® Ruggles®-Redmond™ FDA UDI
Generic Name: Manual surgical saw, flexible FDA UDI
Device Name: Integra® Ruggles®-Redmond™ Bailey-Gigli Saw Guide, 12", Curved FDA UDI
Model / Reference: RN0062 FDA UDI
Description: Integra® Ruggles®-Redmond™ Bailey-Gigli Saw Guide, 12", Curved FDA UDI

Identifiers

Catalog Number: RN0062 FDA UDI
Primary DI / UDI-DI: 10381780229537 FDA UDI
FDA Product Code: GDR FDA UDI
GMDN Term: Manual surgical saw, flexible 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

Yes

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Manual surgical saw, flexible

Integra® Ruggles®-Redmond™ by Integra LifeSciences Production Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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WIRE SAW — KLS-Martin L.P. · Class I
Gigli Saw Handle — N S SURGICAL COMPANY · Class I
Quinelato — Schobell Industrial Ltda · Class I

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: Integra LifeSciences Production Corporation

Sources (1)

FDA UDI b92a88d6-6652-4696-a1c8-c6e25cbf7db1 35 fields · synced Jun 9, 2026