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Handle-Arm Connector Screw

FDA UDI

Class I (US FDA UDI)

by Orthopedic Designs North America, Inc.

Identity

Trade Name
Handle-Arm Connector Screw FDA UDI
Generic Name
Orthopaedic instrument surgical connector FDA UDI
Device Name
Handle-Arm Connector Screw FDA UDI
Model / Reference
ODIT107 FDA UDI
Description
Handle-Arm Connector Screw FDA UDI

Identifiers

Catalog Number
ODI-T107 FDA UDI
Primary DI / UDI-DI
B058ODIT1071 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic instrument surgical connector 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic instrument surgical connector

Handle-Arm Connector Screw by Orthopedic Designs North America, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic instrument surgical connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2869b2fb-b98d-4038-8dd8-a883d40b7d1c 35 fields · synced May 30, 2026