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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
Burring power tool attachment FDA UDI
Device Name
ATT AT10A ANGLED LGND TELESCOPING BASE FDA UDI
Model / Reference
AT10A FDA UDI
Description
ATT AT10A ANGLED LGND TELESCOPING BASE FDA UDI

Identifiers

Primary DI / UDI-DI
00643169181984 FDA UDI
510(k) Number
K020069 FDA UDI
FDA Product Code
HBB FDA UDI
GMDN Term
Burring power tool attachment 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

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: Burring power tool attachment

A comprehensive medical device for neurology, designed to connect to surgical power tool systems and convert non-dedicated mechanical energy to dedicated motion.

Similar devices

Also classified as Burring power tool attachment.

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 53340466-b7a2-40be-9f48-0f9e5367077b 35 fields · synced Jul 6, 2026