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Lag Guide Pin

FDA UDI

Class I (US FDA UDI)

by Orthopedic Designs North America, Inc.

Identity

Trade Name
Lag Guide Pin FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
Lag Guide Pin, 2.4mm X 800mm FDA UDI
Model / Reference
ODID104 FDA UDI
Description
Lag Guide Pin, 2.4mm X 800mm FDA UDI

Identifiers

Catalog Number
ODI-D104 FDA UDI
Primary DI / UDI-DI
B058ODID1041 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic guidewire, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2.4 Millimeter FDA UDI
Length — 800 Millimeter FDA UDI

Category: Orthopaedic guidewire, single-use

Lag Guide Pin by Orthopedic Designs North America, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b92323d1-501f-49b6-a0be-d36f79e1d4ce 36 fields · synced Jun 6, 2026