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Lipogems Process Device 240 S

FDA UDI

Class II (US FDA UDI)

by Lipogems International Spa

Identity

Trade Name
Lipogems Process Device 240 S FDA UDI
Generic Name
Autologous adipose tissue noninvasive processing set FDA UDI
Device Name
Lipogems Process Device 240 Surgery FDA UDI
Model / Reference
LGD 240 FDA UDI
Description
Lipogems Process Device 240 Surgery FDA UDI

Identifiers

Catalog Number
LGD 240 S FDA UDI
Primary DI / UDI-DI
08058773562142 FDA UDI
FDA Product Code
MUU FDA UDI
QKL FDA UDI
GMDN Term
Autologous adipose tissue noninvasive processing set 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Total Volume — 240 Milliliter FDA UDI

Category: Autologous adipose tissue noninvasive processing set

Lipogems Process Device 240 S by Lipogems International Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Autologous adipose tissue noninvasive processing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b182b71c-7f72-4d2a-a533-84a6e2c021f0 37 fields · synced May 31, 2026