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Neptune™ Cable for AquaMic™

FDA UDI

Class III (US FDA UDI)

by Advanced Bionics

Identity

Trade Name
Neptune™ Cable for AquaMic™ FDA UDI
Generic Name
Cochlear implant/auditory brainstem implant coil cable FDA UDI
Device Name
18"White FDA UDI
Model / Reference
CI-5414-503 FDA UDI
Description
18"White FDA UDI

Identifiers

Primary DI / UDI-DI
00840094451216 FDA UDI
PMA Number
P960058 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Cochlear implant/auditory brainstem implant coil cable FDA UDI

Classification

Device Class
Class III 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 46 Centimeter FDA UDI

Category: Cochlear implant/auditory brainstem implant coil cable

Neptune™ Cable for AquaMic™ by Advanced Bionics — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cochlear implant/auditory brainstem implant coil cable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Advanced Bionics

Sources (1)

  • FDA UDI d35886d0-f932-415b-af40-6a02a850277c 37 fields · synced Jun 8, 2026