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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 retraction cannula FDA UDI
Device Name
Sheath 11 mm x 75 mm FDA UDI
Model / Reference
NN-8033 FDA UDI
Description
Sheath 11 mm x 75 mm FDA UDI

Identifiers

Primary DI / UDI-DI
00816744028336 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Neurosurgical retraction cannula 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

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

Category: Neurosurgical retraction cannula

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

Similar devices

Also classified as Neurosurgical retraction cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
NICO Corporation

Sources (1)

  • FDA UDI 99988c41-b35c-40f1-a2a2-5fb4aad620f5 34 fields · synced May 30, 2026