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EarClear Rx

FDA UDI

Class I (US FDA UDI)

by Nuance Medical, Llc

Identity

Trade Name
EarClear Rx FDA UDI
Generic Name
Ear canal irrigation kit, reusable FDA UDI
Device Name
EarClear Rx Ear Wash System Flexible FDA UDI
Model / Reference
90002 FDA UDI
Description
EarClear Rx Ear Wash System Flexible FDA UDI

Identifiers

Catalog Number
90002 FDA UDI
Primary DI / UDI-DI
00856331006187 FDA UDI
FDA Product Code
KCP FDA UDI
GMDN Term
Ear canal irrigation kit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.5220 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ear canal irrigation kit, reusable

EarClear Rx by Nuance Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ear canal irrigation kit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nuance Medical, Llc

Sources (1)

  • FDA UDI 1960acad-f32a-4f52-8ae5-53f1f85b168a 35 fields · synced Jun 6, 2026