Bevel

FDA UDI

Class I (US FDA UDI)

by The Wells Johnson Company

Identity

Trade Name: BEVEL FDA UDI
Generic Name: Liposuction system cannula, reusable FDA UDI
Device Name: Cannula, Bevel, specify length, diameter and handle/hub FDA UDI
Model / Reference: 20121200 FDA UDI
Description: Cannula, Bevel, specify length, diameter and handle/hub FDA UDI

Identifiers

Catalog Number: 20-1212-00 FDA UDI
Primary DI / UDI-DI: B458201212000 FDA UDI
FDA Product Code: GEA FDA UDI
GMDN Term: Liposuction system cannula, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Liposuction system cannula, reusable

Bevel by The Wells Johnson Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: The Wells Johnson Company

Sources (1)

FDA UDI 269520c8-2674-478a-9fcc-702ae8ffaa6f 34 fields · synced Jun 1, 2026