← Back to catalogue

Jackson-Pratt

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
JACKSON-PRATT FDA UDI
Generic Name
Closed-wound drain, non-bioabsorbable FDA UDI
Device Name
JP CHAN DRN SIL RND 15FR 3/4 W/TRO FDA UDI
Model / Reference
JP-2223 FDA UDI
Description
JP CHAN DRN SIL RND 15FR 3/4 W/TRO FDA UDI

Identifiers

Catalog Number
JP-2223 FDA UDI
Primary DI / UDI-DI
10885380182563 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Closed-wound drain, non-bioabsorbable

Jackson-Pratt 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d86878ba-4cad-4549-b7ba-94a7fe3aca74 34 fields · synced Jun 8, 2026