PercuSet Arthrogram Tray

FDA UDI

Class II (US FDA UDI)

by Bracco Diagnostics Inc.

Identity

Trade Name: PercuSet Arthrogram Tray FDA UDI
Generic Name: Aspiration tray, single-use FDA UDI
Device Name: PercuSet Arthrogram Tray FDA UDI
Model / Reference: 600803 FDA UDI
Description: PercuSet Arthrogram Tray FDA UDI

Identifiers

Catalog Number: 600803 FDA UDI
Primary DI / UDI-DI: 10815112021129 FDA UDI
FDA Product Code: OGJ FDA UDI
GMDN Term: Aspiration tray, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5140 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Aspiration tray, single-use

PercuSet Arthrogram Tray by Bracco Diagnostics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Aspiration tray, single-use.

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Turkel — Cardinalhealth · Class II
Safe-T-Centesis — CAREFUSION 2200, INC. · Class II

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: Bracco Diagnostics Inc.

Sources (1)

FDA UDI ce7fb9de-7a3c-482a-ab25-e9148a27e8cb 35 fields · synced May 30, 2026