← Back to catalogue

Midas Rex MR8

FDA UDI

Class II (US FDA UDI)

by Medtronic Powered Surgical Solutions

Identity

Trade Name
Midas Rex MR8 FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
CASE CA875 MR8 INSTRUMENT 3/4 DIN NAVIG FDA UDI
Model / Reference
CA875 FDA UDI
Description
CASE CA875 MR8 INSTRUMENT 3/4 DIN NAVIG FDA UDI

Identifiers

Primary DI / UDI-DI
00643169912205 FDA UDI
510(k) Number
K183644 FDA UDI
FDA Product Code
FMZ FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5400 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Dry Heat Sterilization FDA UDI

Category: Instrument tray, reusable

Midas Rex MR8 by Medtronic Powered Surgical Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 4828b784-88ce-4252-8e3f-87c0261ec471 35 fields · synced Jun 9, 2026