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POWEREASE™ Instruments

FDA UDI

Class II (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
POWEREASE™ Instruments FDA UDI
Generic Name
Surgical power tool system control unit, line-powered FDA UDI
Device Name
CONSOLE 2340000LO POWEREASE IPC LOANER FDA UDI
Model / Reference
2340000LO FDA UDI
Description
CONSOLE 2340000LO POWEREASE IPC LOANER FDA UDI

Identifiers

Primary DI / UDI-DI
00643169288102 FDA UDI
510(k) Number
K111520 FDA UDI
FDA Product Code
GWF FDA UDI
HWE FDA UDI
HBE FDA UDI
GMDN Term
Surgical power tool system control unit, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1870 FDA UDI
878.4820 FDA UDI
882.4310 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

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical power tool system control unit, line-powered

POWEREASE™ Instruments by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool system control unit, line-powered.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d7daf0ac-5035-4f0d-b201-8490e57036f2 35 fields · synced May 30, 2026