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Armada

FDA UDI

Class I (US FDA UDI)

by Nuvasive, Inc.

Identity

Trade Name
Armada FDA UDI
Generic Name
Internal spinal fixation procedure kit, reusable FDA UDI
Device Name
ARM15T Bender, 5.5mm In-Situ Coronal R FDA UDI
Model / Reference
7459032 FDA UDI
Description
ARM15T Bender, 5.5mm In-Situ Coronal R FDA UDI

Identifiers

Primary DI / UDI-DI
00887517484635 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Internal spinal fixation procedure kit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Internal spinal fixation procedure kit, reusable

Armada by Nuvasive, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Internal spinal fixation procedure kit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nuvasive, Inc.

Sources (1)

  • FDA UDI 2a17b1e4-4c5b-4f17-8fac-372fd07adec3 34 fields · synced May 30, 2026