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Fibonacci Lower Extremity Plates Tray

FDA UDI

Class I (US FDA UDI)

by Advanced Orthopaedic Solutions, Inc.

Identity

Trade Name
Fibonacci Lower Extremity Plates Tray FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Model / Reference
9939-000 FDA UDI

Identifiers

Primary DI / UDI-DI
00848665027709 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Instrument tray, 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Fibonacci Lower Extremity Plates Tray by Advanced Orthopaedic Solutions, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b7b3aa40-d737-4ea5-ab29-4be7dc241594 32 fields · synced Jun 8, 2026