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Cochlear™ CP1110S Surgical Coil, 2m

FDA UDI

Class III (US FDA UDI)

by Cochlear

Identity

Trade Name
Cochlear™ CP1110S Surgical Coil, 2m FDA UDI
Generic Name
Cochlear implant intraoperative electrophysiological transceiver FDA UDI
Device Name
Hearing Implant Accessory FDA UDI
Model / Reference
2m FDA UDI
Description
Hearing Implant Accessory FDA UDI

Identifiers

Catalog Number
P1998830 FDA UDI
Primary DI / UDI-DI
09321502073110 FDA UDI
PMA Number
P970051 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Cochlear implant intraoperative electrophysiological transceiver 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cochlear implant intraoperative electrophysiological transceiver

Cochlear™ CP1110S Surgical Coil, 2m by Cochlear — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cochlear implant intraoperative electrophysiological transceiver.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cochlear

Sources (1)

  • FDA UDI de4d9914-09b0-48fb-a1b2-b62ac72e10fe 36 fields · synced May 30, 2026