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Dynesys®

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Dynesys® FDA UDI
Generic Name
Spinal dynamic-stabilization system FDA UDI
Model / Reference
01.03916.455 FDA UDI

Identifiers

Primary DI / UDI-DI
00889024481930 FDA UDI
FDA Product Code
NQP FDA UDI
GMDN Term
Spinal dynamic-stabilization system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 55 Millimeter FDA UDI
Outer Diameter — 6.4 Millimeter FDA UDI

Category: Spinal dynamic-stabilization system

Dynesys® by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal dynamic-stabilization system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI 3f38ecc3-75ea-4535-a96d-04604eb67368 34 fields · synced May 30, 2026