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Wush

FDA UDI

Class I (US FDA UDI)

by Guangdong Okay Technology Co., Ltd.

Identity

Trade Name
WUSH FDA UDI
Generic Name
Ear canal lavage system FDA UDI
Device Name
Wush Powered Ear Cleaner,Black wolf-Wush Rechargeable (Basic, 6 tip, catch cup) This device complies with part 18 of FCC rules. FDA UDI
Model / Reference
WUSH0106,WUSH0706,WUSH0906,WUSH0103,WUSH1012 FDA UDI
Description
Wush Powered Ear Cleaner,Black wolf-Wush Rechargeable (Basic, 6 tip, catch cup) This device complies with part 18 of FCC rules. FDA UDI

Identifiers

Primary DI / UDI-DI
06936189900746 FDA UDI
FDA Product Code
LRD FDA UDI
GMDN Term
Ear canal lavage system 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ear canal lavage system

Wush by Guangdong Okay Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ear canal lavage system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Guangdong Okay Technology Co., Ltd.

Sources (1)

  • FDA UDI c7f1e7f9-fab9-45a9-bc4d-0a3ac0f5a601 34 fields · synced Jun 8, 2026