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MD Resource

FDA UDI

Class II (US FDA UDI)

by Medical Device Resource Corp.

Identity

Trade Name
MD Resource FDA UDI
Generic Name
Liposuction system FDA UDI
Device Name
A standard LS2 Liposuction aspirator accessory. FDA UDI
Model / Reference
FL3000 FDA UDI
Description
A standard LS2 Liposuction aspirator accessory. FDA UDI

Identifiers

Primary DI / UDI-DI
00859898006492 FDA UDI
510(k) Number
K081593 FDA UDI
FDA Product Code
MUU FDA UDI
GMDN Term
Liposuction system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5040 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Liposuction system

MD Resource by Medical Device Resource Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liposuction system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9469ce3e-7b50-4588-bfe2-6d97799e0671 34 fields · synced May 30, 2026