Exchange Tube

FDA UDI

Class I (US FDA UDI)

by Orthopedic Designs North America, Inc.

Identity

Trade Name: Exchange Tube FDA UDI
Generic Name: Orthopaedic implantation sleeve, single-use FDA UDI
Device Name: Guide Wire Exchange Tube FDA UDI
Model / Reference: SLNT44 FDA UDI
Description: Guide Wire Exchange Tube FDA UDI

Identifiers

Catalog Number: SLN-T44 FDA UDI
Primary DI / UDI-DI: B058SLNT441 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Orthopaedic implantation sleeve, 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implantation sleeve, single-use

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Orthopedic Designs North America, Inc.

Sources (1)

FDA UDI 5099f896-6a00-43c1-ac4d-5f802bc112d4 35 fields · synced May 30, 2026