← Back to catalogue

Longeviti Convenience Kit 5.0

FDA UDI

Class II (US FDA UDI)

by Longeviti Neuro Solutions

Identity

Trade Name
Longeviti Convenience Kit 5.0 FDA UDI
Generic Name
Cranial resinous compound FDA UDI
Device Name
ClearFit & InvisiShunt Conveniece Kit FDA UDI
Model / Reference
700075 FDA UDI
Description
ClearFit & InvisiShunt Conveniece Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00855113008661 FDA UDI
FDA Product Code
KKY FDA UDI
GNX FDA UDI
GMDN Term
Cranial resinous compound FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3500 FDA UDI
866.3330 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Polyethylene craniofacial tissue reconstructive materialCranial resinous compound

Longeviti Convenience Kit 5.0 by Longeviti Neuro Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cranial resinous compound.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Longeviti Neuro Solutions

Sources (1)

  • FDA UDI ea128170-5829-4975-bae0-c70435c29d23 33 fields · synced May 30, 2026