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Midas Rex®

FDA UDI

Class II (US FDA UDI)

by Medtronic Powered Surgical Solutions

Identity

Trade Name
Midas Rex® FDA UDI
Generic Name
Manual bone mill FDA UDI
Device Name
CONSOLE BM120-R ELEC BONE MILL REFURB FDA UDI
Model / Reference
BM120-R FDA UDI
Description
CONSOLE BM120-R ELEC BONE MILL REFURB FDA UDI

Identifiers

Primary DI / UDI-DI
00643169999183 FDA UDI
FDA Product Code
HBC FDA UDI
GMDN Term
Manual bone mill FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Category: Manual bone mill

Midas Rex® by Medtronic Powered Surgical Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual bone mill.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 928a946a-e0d1-4657-b1b7-55ebad17e788 35 fields · synced Jun 9, 2026