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Midas Rex Clearview

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
Midas Rex Clearview FDA UDI
Generic Name
Orthopaedic bur, reusable FDA UDI
Device Name
TOOL DC SD12BA40 LGD 12CM DIST 4.0 BALL FDA UDI
Model / Reference
SD12BA40 FDA UDI
Description
TOOL DC SD12BA40 LGD 12CM DIST 4.0 BALL FDA UDI

Identifiers

Primary DI / UDI-DI
00763000892692 FDA UDI
510(k) Number
K081277 FDA UDI
FDA Product Code
ERL FDA UDI
GMDN Term
Orthopaedic bur, reusable 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

Yes

FDA UDI

Single Use

Yes

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, reusable

Midas Rex Clearview by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bur, reusable.

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 c74e25d0-5edf-47f3-bb16-2f4c602621c0 35 fields · synced Jun 6, 2026