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Integra®

FDA UDI

Class II (US FDA UDI)

by Integra Lifesciences Corp.

Identity

Trade Name
Integra® FDA UDI
Generic Name
Ventricular cerebrospinal fluid drainage catheterization kit FDA UDI
Device Name
Integra® EVD System with Burette Sampling FDA UDI
Model / Reference
NL8508502 FDA UDI
Description
Integra® EVD System with Burette Sampling FDA UDI

Identifiers

Catalog Number
NL8508502 FDA UDI
Primary DI / UDI-DI
10381780071686 FDA UDI
510(k) Number
K932769 FDA UDI
K972994 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Ventricular 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: Ventricular cerebrospinal fluid drainage catheterization kit

Integra® 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

K932769 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 791c6249-5c49-4f3a-9b1e-012f8d54c2bf 37 fields · synced May 30, 2026