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Distraction Tube - Right

FDA UDI

Class I (US FDA UDI)

by Highridge Medical, LLC

Identity

Trade Name
Distraction Tube - Right FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
DISTRACTION TUBE - RIGHT FDA UDI
Model / Reference
LV01291 FDA UDI
Description
DISTRACTION TUBE - RIGHT FDA UDI

Identifiers

Catalog Number
LV01291 FDA UDI
Primary DI / UDI-DI
00880304855403 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, 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

No

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

No

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: Orthopaedic surgical procedure kit, non-medicated, reusable

Distraction Tube - Right by Highridge Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Highridge Medical, LLC

Sources (1)

  • FDA UDI 676999d2-517d-45ec-abf1-c4d0bae686f2 35 fields · synced Jun 8, 2026