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Slim HP AquaMic™

FDA UDI

Class III (US FDA UDI)

by Advanced Bionics

Identity

Trade Name
Slim HP AquaMic™ FDA UDI
Generic Name
Cochlear implant/auditory brainstem implant coil FDA UDI
Device Name
24" Brown FDA UDI
Model / Reference
CI-5321-011 FDA UDI
Description
24" Brown FDA UDI

Identifiers

Primary DI / UDI-DI
00840094446502 FDA UDI
PMA Number
P960058 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Cochlear implant/auditory brainstem implant coil 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
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 61 Centimeter FDA UDI

Category: Cochlear implant/auditory brainstem implant coil

Slim HP 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.

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 8b90a05b-1c5b-43fa-be72-d3cf31ed3676 37 fields · synced May 30, 2026