← Back to catalogue

Midas Rex

FDA UDI

Class II (US FDA UDI)

by Medtronic Powered Surgical Solutions

Identity

Trade Name
Midas Rex FDA UDI
Generic Name
Orthopaedic bur, single-use FDA UDI
Device Name
TOOL 9MH30D LEGEND 9CM 3MM MH DIAM FDA UDI
Model / Reference
9MH30D FDA UDI
Description
TOOL 9MH30D LEGEND 9CM 3MM MH DIAM FDA UDI

Identifiers

Primary DI / UDI-DI
00643169760912 FDA UDI
510(k) Number
K020069 FDA UDI
FDA Product Code
HBB FDA UDI
GMDN Term
Orthopaedic bur, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic bur, single-use

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

Similar devices

Also classified as Orthopaedic bur, single-use.

Cleared under the same submission

K020069 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medtronic Powered Surgical Solutions

Sources (1)

  • FDA UDI 196f74dc-1dae-4c86-a16b-695a9b35a01c 35 fields · synced Jun 9, 2026