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Midas Rex™

FDA UDI

Class I (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
BLADE 208F1SS TRITON SAGI 19.1MMX 41MM FDA UDI
Model / Reference
208F1SS FDA UDI
Description
BLADE 208F1SS TRITON SAGI 19.1MMX 41MM FDA UDI

Identifiers

Primary DI / UDI-DI
00643169796980 FDA UDI
510(k) Number
K870157 FDA UDI
FDA Product Code
KFK FDA UDI
GMDN Term
Orthopaedic bur, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Category: Orthopaedic bur, single-use

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

Similar devices

Also classified as Orthopaedic bur, single-use.

Cleared under the same submission

K870157 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic Powered Surgical Solutions

Sources (1)

  • FDA UDI 38a341d1-0d66-42e8-beee-bcbc37c07084 35 fields · synced Jun 9, 2026