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ClearLook Lighted InfantScoop, Refill

FDA UDI

Class I (US FDA UDI)

by Bionix, LLC

Identity

Trade Name
ClearLook Lighted InfantScoop, Refill FDA UDI
Generic Name
ENT illuminating foreign body extraction set FDA UDI
Device Name
ClearLook Lighted InfantScoop, 50ct Refill FDA UDI
Model / Reference
3460 FDA UDI
Description
ClearLook Lighted InfantScoop, 50ct Refill FDA UDI

Identifiers

Catalog Number
3460 FDA UDI
Primary DI / UDI-DI
00714646001351 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 Lighted InfantScoop, Refill 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 e1ee8816-4bff-425e-bf45-4e59ca2c8286 35 fields · synced May 30, 2026