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Lipogems Process Device

by Lipogems International S.p.A.

Ref LGD 120 B, LGD 240 B, LGD 60 S, LGD 120 S, LGD 60 B, LGD 240 M, LGD 240 O, LGD 120 M

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number8058773560001LGDU2 Basic UDI-DI Date8 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08058773562746 UDI-DI Date16 Sep 2016ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Lipogems Process Device EUDAMED
Lipogems Process Device 60 B GUDID
Lipogems Process Device 240 O GUDID
Lipogems Process Device 240 M GUDID
Lipogems Process Device 240 B GUDID
Lipogems Process Device 120 M GUDID
Lipogems Process Device 120 S GUDID
Lipogems Process Device 60 S GUDID
Lipogems Process Device 120 B GUDID
Generic Name
Autologous adipose tissue noninvasive processing set
Model / Ref / Catalog
LGD 120 B, LGD 240 B, LGD 60 S, LGD 120 S, LGD 60 B, LGD 240 M, LGD 240 O, LGD 120 M, LGD 60, LGD 240, LGD 120
Primary DI / UDI-DI
08058773562746, 08058773562197, 08058773562166, 08058773562432, 08058773562180, 08058773562753, 08058773562777, 08058773562159
Basic UDI-DI
8058773560001LGDU2
FDA Product Code
MUU, QKL
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
GMDN Term
Autologous adipose tissue noninvasive processing set
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
878.5040
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 60 Milliliter
Total Volume — 240 Milliliter
Total Volume — 120 Milliliter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
LGD 120 B
LGD 240 B
LGD 60 S
LGD 120 S
LGD 60 B
LGD 240 M
LGD 240 O
LGD 120 M
GUDID
LGD 60
LGD 240
LGD 120
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
IT-MF-000010159

Related devices

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (18)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No