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Billeau Ear Loop/Curette

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
BILLEAU EAR LOOP/CURETTE FDA UDI
Generic Name
Ear snare FDA UDI
Device Name
BILLEAU EAR LOOP/CURETTE LARGE LOOP FDA UDI
Model / Reference
467-436 FDA UDI
Description
BILLEAU EAR LOOP/CURETTE LARGE LOOP FDA UDI

Identifiers

Catalog Number
467-436 FDA UDI
Primary DI / UDI-DI
00192896040137 FDA UDI
FDA Product Code
JYL FDA UDI
GMDN Term
Ear snare 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

No

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

No

FDA UDI

Dimensions & Sizes

Size
Length — 6.5 Inch FDA UDI

Category: Ear snare

Billeau Ear Loop/Curette by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ear snare.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a22392de-9e19-449e-89ad-cf08543d1c76 36 fields · synced Jun 6, 2026