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1/4 Square Adaptor

FDA UDI

Class I (US FDA UDI)

by Highridge Medical, LLC

Identity

Trade Name
1/4 Square Adaptor FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
1/4 SQUARE ADAPTOR FDA UDI
Model / Reference
LV00901 FDA UDI
Description
1/4 SQUARE ADAPTOR FDA UDI

Identifiers

Catalog Number
LV00901 FDA UDI
Primary DI / UDI-DI
00888480588177 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic inorganic implant inserter/extractor, 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 inorganic implant inserter/extractor, reusable

1/4 Square Adaptor by Highridge Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic inorganic implant inserter/extractor, 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 5f70e023-1725-4e09-a56a-ccb806399524 35 fields · synced May 30, 2026