← 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
Pneumatic surgical power tool hose FDA UDI
Device Name
ACCY PC220 LEGEND 20 FT EXTENSION HOSE FDA UDI
Model / Reference
PC220 FDA UDI
Description
ACCY PC220 LEGEND 20 FT EXTENSION HOSE FDA UDI

Identifiers

Primary DI / UDI-DI
00763000080143 FDA UDI
510(k) Number
K163182 FDA UDI
FDA Product Code
HBB FDA UDI
GMDN Term
Pneumatic surgical power tool hose 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
High-level Disinfectant FDA UDI

Category: Pneumatic surgical power tool hose

Midas Rex by Medtronic Powered Surgical Solutions — Class II — 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

K163182 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 d761a7c4-5591-4a75-ab0d-97b52c360af1 35 fields · synced Jun 9, 2026