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KYPHON ELEMENT™ Balloon Kyphoplasty System

FDA UDI

Class II (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
KYPHON ELEMENT™ Balloon Kyphoplasty System FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
INFLATION SYRINGE A25R VALUE SYRINGE FDA UDI
Model / Reference
A25R FDA UDI
Description
INFLATION SYRINGE A25R VALUE SYRINGE FDA UDI

Identifiers

Primary DI / UDI-DI
00643169582224 FDA UDI
510(k) Number
K994253 FDA UDI
FDA Product Code
DXT FDA UDI
GMDN Term
General-purpose syringe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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

Yes

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: General-purpose syringe, single-use

KYPHON ELEMENT™ Balloon Kyphoplasty System by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe, single-use.

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 3d6f7db0-45b0-480d-8487-b815f0d42041 35 fields · synced Jun 8, 2026