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Medtronic Reusable Instruments

FDA UDI

Class I (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
Medtronic Reusable Instruments FDA UDI
Generic Name
Orthopaedic cement dispenser FDA UDI
Device Name
CEMENT GUN AND BONE FILLER CDS2A SISE 2 FDA UDI
Model / Reference
CDS2A FDA UDI
Description
CEMENT GUN AND BONE FILLER CDS2A SISE 2 FDA UDI

Identifiers

Primary DI / UDI-DI
00643169100749 FDA UDI
FDA Product Code
KIH FDA UDI
GMDN Term
Orthopaedic cement dispenser FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4200 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

No

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

Category: Orthopaedic cement dispenser

Medtronic Reusable Instruments by Medtronic Sofamor Danek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic cement dispenser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fee38a9a-ec82-4428-b38c-f3192a1dba75 34 fields · synced Jun 1, 2026