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NICO BrainPath

FDA UDI

Class II (US FDA UDI)

by NICO Corporation

Identity

Trade Name
NICO BrainPath FDA UDI
Generic Name
Neurosurgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Kit - 13.5 mm x 95 mm Upgrade FDA UDI
Model / Reference
NN-7043 FDA UDI
Description
Kit - 13.5 mm x 95 mm Upgrade FDA UDI

Identifiers

Primary DI / UDI-DI
00816744027438 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Neurosurgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Neurosurgical procedure kit, non-medicated, reusable

NICO BrainPath by NICO Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
NICO Corporation

Sources (1)

  • FDA UDI 43339b15-88ec-4b30-9502-23f72690ce76 34 fields · synced May 31, 2026