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XPS® Micro

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
XPS® Micro FDA UDI
Generic Name
Surgical power tool system control unit, pneumatic FDA UDI
Device Name
CONSOLE 1894440 XPS MICRO MICRODEBRIDER FDA UDI
Model / Reference
1894440 FDA UDI
Description
CONSOLE 1894440 XPS MICRO MICRODEBRIDER FDA UDI

Identifiers

Primary DI / UDI-DI
00721902773013 FDA UDI
510(k) Number
K002224 FDA UDI
FDA Product Code
ERL FDA UDI
GMDN Term
Surgical power tool system control unit, pneumatic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 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

Category: Surgical power tool system control unit, pneumatic

XPS® Micro by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool system control unit, pneumatic.

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 1cd8edb1-5bae-40d7-b9d9-43d8e4b3b7c6 36 fields · synced Jun 1, 2026