Integra® Ruggles®-Redmond™

FDA UDI

Class II (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name: Integra® Ruggles®-Redmond™ FDA UDI
Generic Name: Suction system catheter, general-purpose FDA UDI
Device Name: Integra® Ruggles®-Redmond™ Atraumatic Suction Tube, 5-3/8" working length, Multi-Hole malleable angled, 5 French FDA UDI
Model / Reference: R0675 FDA UDI
Description: Integra® Ruggles®-Redmond™ Atraumatic Suction Tube, 5-3/8" working length, Multi-Hole malleable angled, 5 French FDA UDI

Identifiers

Catalog Number: R0675 FDA UDI
Primary DI / UDI-DI: 10381780131113 FDA UDI
FDA Product Code: JOL FDA UDI
GMDN Term: Suction system catheter, general-purpose FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6740 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: Suction system catheter, general-purpose

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

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Novo Surgical Inc. — NOVO SURGICAL, INC. · 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 II	Pending data

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Manufacturer

Manufacturer: Integra LifeSciences Production Corporation

Sources (1)

FDA UDI e98e04d3-9f21-4807-8bd3-2352f6e4922d 35 fields · synced Jun 9, 2026