Instrument

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name: INSTRUMENT FDA UDI
Generic Name: Bone lever/elevator, reusable FDA UDI
Device Name: MIS. FEMORAL ELEVATOR FOR ANTERIOR APPROACH FDA UDI
Model / Reference: 4849-8-005 FDA UDI
Description: MIS. FEMORAL ELEVATOR FOR ANTERIOR APPROACH FDA UDI

Identifiers

Catalog Number: 4849-8-005 FDA UDI
Primary DI / UDI-DI: 07613327192452 FDA UDI
FDA Product Code: LPH FDA UDI
MBL FDA UDI
MEH FDA UDI
MAY FDA UDI
LZO FDA UDI
GMDN Term: Bone lever/elevator, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3358 FDA UDI
888.3353 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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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

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Combination Product

FDA UDI

HCT/P

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Premarket Exempt

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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: Bone lever/elevator, reusable

Instrument by Howmedica Osteonics Corp. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Howmedica Osteonics Corp.

Sources (1)

FDA UDI 404892c5-1006-40af-bf70-85e7b03ecfa7 34 fields · synced May 30, 2026