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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
Pneumatic surgical power tool hose FDA UDI
Device Name
HOSE PC710 MR7/MR8 REGULATOR PNEUMATICA^ FDA UDI
Model / Reference
PC710 FDA UDI
Description
HOSE PC710 MR7/MR8 REGULATOR PNEUMATICA^ FDA UDI

Identifiers

Primary DI / UDI-DI
00763000080174 FDA UDI
510(k) Number
K183515 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Pneumatic surgical power tool hose FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 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

Category: Pneumatic surgical power tool hose

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

Similar devices

Also classified as Pneumatic surgical power tool hose.

Cleared under the same submission

K183515 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 36ad28f1-d9b3-4573-8708-d8a33e984622 35 fields · synced Jun 9, 2026