← Back to catalogue

Lucid®

FDA UDI

Class I (US FDA UDI)

by Hearing Lab Technology, Llc

Identity

Trade Name
Lucid® FDA UDI
Generic Name
Air-conduction hearing aid acoustic tube FDA UDI
Device Name
Enrich Pro BTE OTC FDA UDI
Model / Reference
Enrich Pro BTE FDA UDI
Description
Enrich Pro BTE OTC FDA UDI

Identifiers

Catalog Number
10082 FDA UDI
Primary DI / UDI-DI
00810068831443 FDA UDI
FDA Product Code
QUF FDA UDI
GMDN Term
Air-conduction hearing aid acoustic tube FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.3300 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Air-conduction hearing aid acoustic tube

Lucid® by Hearing Lab Technology, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Air-conduction hearing aid acoustic tube.

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
Hearing Lab Technology, Llc

Sources (1)

  • FDA UDI b21cb9d9-dec5-4009-98e7-3b0c67697da1 35 fields · synced May 30, 2026