MSI Precision Specialty Instruments

FDA UDI

Class I (US FDA UDI)

by Med Saver, Inc.

Identity

Trade Name: MSI Precision Specialty Instruments FDA UDI
Generic Name: Orthopaedic surgical distractor, internal FDA UDI
Device Name: Cervical Vertebral Body Distractor, Right, For Use In Procedures From The Right Approach For C5 Through T1/2, From The Left Approach For The Upper Cervical Spine FDA UDI
Model / Reference: 66-902AES FDA UDI
Description: Cervical Vertebral Body Distractor, Right, For Use In Procedures From The Right Approach For C5 Through T1/2, From The Left Approach For The Upper Cervical Spine FDA UDI

Identifiers

Primary DI / UDI-DI: 00194613120740 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Orthopaedic surgical distractor, internal 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

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Prescription Use

Yes

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Over-the-Counter

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Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

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Premarket Exempt

Yes

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Lot / Batch Number

Yes

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Serial Number

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Expiration Date

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Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic surgical distractor, internal

MSI Precision Specialty Instruments by Med Saver, 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: Med Saver, Inc.

Sources (1)

FDA UDI 94c1ebf2-4738-48c2-ac9b-eacb2eb44645 34 fields · synced May 30, 2026