Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name: CARDINAL HEALTH FDA UDI
Generic Name: Closed-wound drain, non-bioabsorbable FDA UDI
Device Name: JPH 10FR RND,FULL DUCT, W/TRO FDA UDI
Model / Reference: JP-HUR870 FDA UDI
Description: JPH 10FR RND,FULL DUCT, W/TRO FDA UDI

Identifiers

Catalog Number: JP-HUR870 FDA UDI
Primary DI / UDI-DI: 00192253022172 FDA UDI
FDA Product Code: GBX FDA UDI
GMDN Term: Closed-wound drain, non-bioabsorbable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4200 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

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Closed-wound drain, non-bioabsorbable

Cardinal Health by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound drain, non-bioabsorbable.

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Drainage Tube and Accessories — Hangzhou Fushan Medical Appliances Co., Ltd. · Class IIa
Exodus — NAVILYST MEDICAL, INC. · Class II
One-Step™ — Merit Medical Systems, Inc. · Class I
Aspen® Discrete Drain — Aspen Surgical Products, Inc. · Class I

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: Cardinal Health 200, LLC

Sources (1)

FDA UDI 147eb39e-9988-4441-8796-1c96e559a6c0 34 fields · synced Jun 7, 2026