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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
Neurosurgical bone flap elevator FDA UDI
Device Name
Integra® Ruggles®-Redmond™ Adson Periosteal Elevator, 6-3/4", 9.3mm Wide, Straight, Chisel Edge FDA UDI
Model / Reference
R0260 FDA UDI
Description
Integra® Ruggles®-Redmond™ Adson Periosteal Elevator, 6-3/4", 9.3mm Wide, Straight, Chisel Edge FDA UDI

Identifiers

Catalog Number
R0260 FDA UDI
Primary DI / UDI-DI
10381780222255 FDA UDI
FDA Product Code
GEG FDA UDI
GMDN Term
Neurosurgical bone flap elevator 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Neurosurgical bone flap elevator

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

Similar devices

Also classified as Neurosurgical bone flap elevator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra LifeSciences Production Corporation

Sources (1)

  • FDA UDI 33547d96-7c17-4aa0-bb7a-d15525920293 35 fields · synced Jun 9, 2026