← Back to catalogue

Mas Plif

FDA UDI

Class I (US FDA UDI)

by Nuvasive, Inc.

Identity

Trade Name
MAS PLIF FDA UDI
Generic Name
Internal spinal fixation procedure kit, reusable FDA UDI
Device Name
MAS PLIF Loading Block, Screw Assembly FDA UDI
Model / Reference
7070110 FDA UDI
Description
MAS PLIF Loading Block, Screw Assembly FDA UDI

Identifiers

Primary DI / UDI-DI
00887517414472 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

Mas Plif 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Nuvasive, Inc.

Sources (1)

  • FDA UDI 4f78d98e-8f94-439d-bdb3-6e343aeb4b77 34 fields · synced Jun 8, 2026