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ClearLook™ Sample Pack-Curettes Only

FDA UDI

Class I (US FDA UDI)

by Bionix, LLC

Identity

Trade Name
ClearLook™ Sample Pack-Curettes Only FDA UDI
Generic Name
ENT illuminating foreign body extraction set FDA UDI
Device Name
ClearLook™ Sample Pack-Curettes Only FDA UDI
Model / Reference
23300 FDA UDI
Description
ClearLook™ Sample Pack-Curettes Only FDA UDI

Identifiers

Catalog Number
23300 FDA UDI
Primary DI / UDI-DI
00714646000897 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

ClearLook™ Sample Pack-Curettes Only 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 319bdd90-be91-4e3d-98e5-0c78ba88f7f5 35 fields · synced May 30, 2026