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Integra

FDA UDI

by Integra Pain Management

Identity

Trade Name
Integra FDA UDI
Generic Name
Ventricular cerebrospinal fluid drainage catheterization kit FDA UDI
Device Name
Combo Kit Consists OF 10-140/10-560/INS-5010 FDA UDI
Model / Reference
31127 FDA UDI
Description
Combo Kit Consists OF 10-140/10-560/INS-5010 FDA UDI

Identifiers

Primary DI / UDI-DI
10381780178187 FDA UDI
GMDN Term
Ventricular cerebrospinal fluid drainage catheterization kit FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

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 kitManual cranial rotary handpiece, single-use

Integra by Integra Pain Management — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual cranial rotary handpiece, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra Pain Management

Sources (1)

  • FDA UDI a1b20835-b1e8-48bb-94ee-e515c24b1820 35 fields · synced Jun 9, 2026