Life Instruments

FDA UDI

Class I (US FDA UDI)

by Life Instrument Corporation

Identity

Trade Name: Life Instruments FDA UDI
Generic Name: Bone curette, reusable FDA UDI
Device Name: #3 Cup Curette lateral left FDA UDI
Model / Reference: 717-1203-4-1 FDA UDI
Description: #3 Cup Curette lateral left FDA UDI

Identifiers

Primary DI / UDI-DI: M9307171203410 FDA UDI
FDA Product Code: FZS FDA UDI
GMDN Term: Bone curette, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

FDA UDI

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 curette, reusable

Life Instruments by Life Instrument Corporation — 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: Life Instrument Corporation

Sources (1)

FDA UDI 490644ca-3a21-4e73-a379-ea1db0007aa6 33 fields · synced May 30, 2026