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Rad®

FDA UDI

Class I (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
RAD® FDA UDI
Generic Name
Surgical saw blade, oscillating, single-use FDA UDI
Device Name
BLADE 1884012 RAD12 5PK CURVED 4MM FDA UDI
Model / Reference
1884012 FDA UDI
Description
BLADE 1884012 RAD12 5PK CURVED 4MM FDA UDI

Identifiers

Primary DI / UDI-DI
20681490047535 FDA UDI
FDA Product Code
EQJ FDA UDI
GMDN Term
Surgical saw blade, oscillating, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4140 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Angle — 12.0 degree FDA UDI
Length — 11.0 Centimeter FDA UDI
Outer Diameter — 4.0 Millimeter FDA UDI

Category: Surgical saw blade, oscillating, single-use

Rad® by Medtronic Xomed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, oscillating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic Xomed, Inc.

Sources (1)

  • FDA UDI 3af6f2a1-dfbd-46fb-968a-0c2fad1c3ebb 35 fields · synced May 30, 2026