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EndoLIF®

FDA UDI

Class I (US FDA UDI)

by Joimax, Inc.

Identity

Trade Name
EndoLIF® FDA UDI
Generic Name
Internal spinal fixation procedure kit, reusable FDA UDI
Device Name
EndoLIF® Instrument Set FDA UDI
Model / Reference
ENDOLIF2 FDA UDI
Description
EndoLIF® Instrument Set FDA UDI

Identifiers

Catalog Number
ENDOLIF2 FDA UDI
Primary DI / UDI-DI
04250337108610 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Internal spinal fixation procedure kit, reusable

EndoLIF® by Joimax, 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
Joimax, Inc.

Sources (1)

  • FDA UDI 4caece43-a879-4ced-8fba-a2e503b20683 36 fields · synced May 30, 2026