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Lighted Articulating - Sample

FDA UDI

Class I (US FDA UDI)

by Bionix, LLC

Identity

Trade Name
Lighted Articulating - Sample FDA UDI
Generic Name
ENT illuminating foreign body extraction set FDA UDI
Device Name
Lighted Articulating Curette - Sample FDA UDI
Model / Reference
22511 FDA UDI
Description
Lighted Articulating Curette - Sample FDA UDI

Identifiers

Catalog Number
22511 FDA UDI
Primary DI / UDI-DI
00714646001252 FDA UDI
FDA Product Code
JYG FDA UDI
GMDN Term
ENT illuminating foreign body extraction set 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: ENT illuminating foreign body extraction set

Lighted Articulating - Sample by Bionix, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT illuminating foreign body extraction set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bionix, LLC

Sources (1)

  • FDA UDI 72321d73-8376-4485-ba95-d6596c20ee7e 35 fields · synced Jun 1, 2026