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Liposuction Cannula

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
LIPOSUCTION CANNULA FDA UDI
Generic Name
Liposuction system cannula, reusable FDA UDI
Device Name
LIPOSUCTION CANNULA SPATULATED TIP FDA UDI
Model / Reference
201-360 FDA UDI
Description
LIPOSUCTION CANNULA SPATULATED TIP FDA UDI

Identifiers

Primary DI / UDI-DI
B0992013600 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Liposuction system cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
Not 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

Liposuction Cannula by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e710452d-88b6-4e5f-8410-2105da4eeab0 36 fields · synced Jun 1, 2026