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Baria

FDA UDI

Class I (US FDA UDI)

by Shenzhen Baria Technology CO., Ltd

Identity

Trade Name
Baria FDA UDI
Generic Name
Ear canal lavage system FDA UDI
Device Name
Ear Cleaner FDA UDI
Model / Reference
EC005 FDA UDI
Description
Ear Cleaner FDA UDI

Identifiers

Primary DI / UDI-DI
06978213840116 FDA UDI
FDA Product Code
KYZ FDA UDI
GMDN Term
Ear canal lavage system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6960 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ear canal lavage system

Baria by Shenzhen Baria 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
Shenzhen Baria Technology CO., Ltd

Sources (1)

  • FDA UDI 0ee85078-0ae2-4f85-aa52-4975d8f5560c 33 fields · synced Jun 1, 2026