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Distal Radius and Forearm Tray

FDA UDI

Class II (US FDA UDI)

by Avanti Orthopaedics Llc

Identity

Trade Name
Distal Radius and Forearm Tray FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Distal Radius and Forearm Tray FDA UDI
Model / Reference
DRFT FDA UDI
Description
Distal Radius and Forearm Tray FDA UDI

Identifiers

Primary DI / UDI-DI
00810054091226 FDA UDI
510(k) Number
K191118 FDA UDI
FDA Product Code
HRS FDA UDI
HWC FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
888.3040 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

No

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

Distal Radius and Forearm Tray by Avanti Orthopaedics Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9e6d3d91-a477-44b3-8c3c-5e26fb1ffa7b 35 fields · synced May 29, 2026