Keos Lumbar Instrument

FDA UDI

Class I (US FDA UDI)

by Keos

Identity

Trade Name: Keos Lumbar Instrument FDA UDI
Generic Name: Bone file/rasp, manual, reusable FDA UDI
Model / Reference: Rasp, Angled, Bayoneted FDA UDI

Identifiers

Catalog Number: 200-36-0006 FDA UDI
Primary DI / UDI-DI: B0842003600060 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Bone file/rasp, manual, reusable 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

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

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone file/rasp, manual, reusable

Keos Lumbar Instrument by Keos — 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: Keos

Sources (1)

FDA UDI e8cd918f-d5ba-44d7-9106-ec93564c05c3 33 fields · synced May 30, 2026