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Midas Rex MR8

FDA UDI

Class II (US FDA UDI)

by Medtronic PS Medical

Identity

Trade Name
Midas Rex MR8 FDA UDI
Generic Name
Surgical power tool system control unit, line-powered FDA UDI
Device Name
MOTOR EM810-R MR8 ELECTRIC TOUCH REFURB FDA UDI
Model / Reference
EM810-R FDA UDI
Description
MOTOR EM810-R MR8 ELECTRIC TOUCH REFURB FDA UDI

Identifiers

Primary DI / UDI-DI
00763000063344 FDA UDI
510(k) Number
K183515 FDA UDI
FDA Product Code
ERL FDA UDI
HBC FDA UDI
GMDN Term
Surgical power tool system control unit, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 FDA UDI
882.4360 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

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

Midas Rex MR8 by Medtronic PS Medical — 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 730de4d9-f1a6-499c-bf77-733e3390feb5 35 fields · synced Jun 1, 2026