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MoniTorr™

FDA UDI

Class II (US FDA UDI)

by Integra Lifesciences Corp.

Identity

Trade Name
MoniTorr™ FDA UDI
Generic Name
Lumbar cerebrospinal fluid drainage catheterization kit FDA UDI
Device Name
MoniTorr™ ICP External CSF Drainage and Monitoring System FDA UDI
Model / Reference
SP0090 FDA UDI
Description
MoniTorr™ ICP External CSF Drainage and Monitoring System FDA UDI

Identifiers

Catalog Number
SP0090 FDA UDI
Primary DI / UDI-DI
10381780071921 FDA UDI
510(k) Number
K022554 FDA UDI
K062599 FDA UDI
K191684 FDA UDI
K920156 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Lumbar cerebrospinal fluid drainage catheterization kit 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lumbar cerebrospinal fluid drainage catheterization kitVentricular cerebrospinal fluid drainage catheterization kit

MoniTorr™ by Integra Lifesciences Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventricular cerebrospinal fluid drainage catheterization kit.

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 f73270cb-5750-47a7-844d-e74c5a2401ad 36 fields · synced May 30, 2026