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Sample, Safe Ear Curette Rainbow Pack

FDA UDI

Class I (US FDA UDI)

by Bionix, LLC

Identity

Trade Name
Sample, Safe Ear Curette Rainbow Pack FDA UDI
Generic Name
Endaural wax extraction curette FDA UDI
Device Name
Sample, Safe Ear Curette Rainbow Pack FDA UDI
Model / Reference
25777-9 FDA UDI
Description
Sample, Safe Ear Curette Rainbow Pack FDA UDI

Identifiers

Catalog Number
25777-9 FDA UDI
Primary DI / UDI-DI
00714646000569 FDA UDI
FDA Product Code
JYG FDA UDI
GMDN Term
Endaural wax extraction curette FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

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: Endaural wax extraction curette

Sample, Safe Ear Curette Rainbow Pack by Bionix, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endaural wax extraction curette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bionix, LLC

Sources (1)

  • FDA UDI 25558684-1b2f-4909-ae61-cab017e4e7cb 35 fields · synced May 30, 2026