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FillerCollector

by Human Med AG

Ref 660000

FillerCollector (660000) is a device classified as Class IIa in the EU and Class II in the US made by Human Med AG, registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI B-04260170881366) and listed in FDA GUDID since 30 Jul 2025 (UDI-DI 04260170881366), active as of 7 Nov 2026.

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

CE MDD

Valid until

No date given

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

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04260170881366 Basic UDI-DI 04260170881366UDI-DIDate2 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04260170881366 UDI-DI Date30 Jul 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04260170881366 registered 2 Nov 2026 Active
  • FDA GUDID UDI-DI 04260170881366 listed 30 Jul 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04260170881366
  2. Registered EUDAMED B-04260170881366

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Generic name
Surgical suction system collection container, reusable
Model / Ref / Catalog
660000, Re-usable FillerCollector, Complete, Collect Fat
Primary DI / UDI-DI
04260170881366
Basic UDI-DI
B-04260170881366
FDA product code
QKL
EMDN code
A060399 Fluid collection bags and systems - other
GMDN term
Surgical suction system collection container, reusable
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
878.5040
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
660000
GUDID
Re-usable FillerCollector, Complete, Collect Fat
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Surgical suction system collection container, reusable

Similar devices in this category

Other devices filed under FLUID COLLECTION BAGS AND SYSTEMS - OTHER.

Other devices from Human Med AG

See all devices from Human Med AG →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Serial number
Other properties (19, all answered No)