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Codman® Hakim® Bactiseal®

FDA UDI

Class II (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
CODMAN® HAKIM® BACTISEAL® FDA UDI
Generic Name
Intracerebral infusion/drainage catheter, short-term FDA UDI
Device Name
CODMAN® HAKIM® BACTISEAL® Shunt System Clear with Barium Stripe Peritoneal Catheter 120cm, with Drainage Holes and Markings FDA UDI
Model / Reference
NS5524 FDA UDI
Description
CODMAN® HAKIM® BACTISEAL® Shunt System Clear with Barium Stripe Peritoneal Catheter 120cm, with Drainage Holes and Markings FDA UDI

Identifiers

Catalog Number
NS5524 FDA UDI
Primary DI / UDI-DI
10381780526797 FDA UDI
FDA Product Code
HCA FDA UDI
GMDN Term
Intracerebral infusion/drainage catheter, short-term FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4100 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 120 Centimeter FDA UDI

Category: Intracerebral infusion/drainage catheter, short-term

Codman® Hakim® Bactiseal® by Integra LifeSciences Production Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intracerebral infusion/drainage catheter, short-term.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra LifeSciences Production Corporation

Sources (1)

  • FDA UDI 62017053-7205-4305-a9d9-6e15f55054c5 37 fields · synced Jun 9, 2026