← Back to catalogue

Esteem® Subdural Needle Electrode

FDA UDI

Class III (US FDA UDI)

by Envoy Medical Corporation

Identity

Trade Name
Esteem® Subdural Needle Electrode FDA UDI
Generic Name
Fully-implantable middle ear implant system FDA UDI
Device Name
Subdural Needle Electrode FDA UDI
Model / Reference
1740 FDA UDI
Description
Subdural Needle Electrode FDA UDI

Identifiers

Catalog Number
701740-002 FDA UDI
Primary DI / UDI-DI
00812282020559 FDA UDI
PMA Number
P090018 FDA UDI
FDA Product Code
OAF FDA UDI
GMDN Term
Fully-implantable middle ear implant system FDA UDI

Classification

Device Class
Class III 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

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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Fully-implantable middle ear implant system

Esteem® Subdural Needle Electrode by Envoy Medical Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fully-implantable middle ear implant system.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 21edc2e6-1f50-43e9-b69b-3d12f01d83e8 36 fields · synced Jun 8, 2026