Integra Peritoneal Open-Ended Catheter With Slits

FDA UDI

Class II (US FDA UDI)

by Integra Lifesciences Corp.

Identity

Trade Name: Integra Peritoneal Open-Ended Catheter With Slits FDA UDI
Generic Name: Peritoneal/atrial cerebrospinal fluid catheter FDA UDI
Device Name: Integra Peritoneal Open-Ended Catheter With Slits PERITONEAL CATHETER, 90CM LENGTH 12 mm H2O at a flow rate of 23 ml/hr. FDA UDI
Model / Reference: NL98003S01 FDA UDI
Description: Integra Peritoneal Open-Ended Catheter With Slits PERITONEAL CATHETER, 90CM LENGTH 12 mm H2O at a flow rate of 23 ml/hr. FDA UDI

Identifiers

Catalog Number: NL98003S01 FDA UDI
Primary DI / UDI-DI: 10381780072546 FDA UDI
FDA Product Code: JXG FDA UDI
GMDN Term: Peritoneal/atrial cerebrospinal fluid catheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.5550 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Peritoneal/atrial cerebrospinal fluid catheter

Integra Peritoneal Open-Ended Catheter With Slits by Integra Lifesciences Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peritoneal/atrial cerebrospinal fluid catheter.

AESCULAP — Christoph Miethke GmbH & Co. KG · Class II
CODMAN® BACTISEAL® — Integra LifeSciences Production Corporation · Class II
CODMAN® ACCU-FLO® — Integra LifeSciences Production Corporation · Class II
Phoenix Neuro — Sophysa SA · Class II
Natus® — Natus Medical Incorporated · Class II
CODMAN® — Integra LifeSciences Production Corporation · Class II
CODMAN® ACCU-FLO® — Integra LifeSciences Production Corporation · Class II
Natus® — Natus Medical Incorporated · 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

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

Manufacturer

Manufacturer: Integra Lifesciences Corp.

Sources (1)

FDA UDI 7bc1581d-820c-470c-9e15-7f1d213c5c33 36 fields · synced May 29, 2026