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FillerCollector

by Human Med AG

FillerCollector (1660000-5) is a Class II device made by Human Med AG, listed in FDA GUDID since 30 Jul 2025 (UDI-DI 04260170881083), registry data as of 1 Jun 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 1 Jun 2026.

Regulatory status

as of registry sync 1 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04260170881083 UDI-DI Date30 Jul 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Surgical suction system collection container, single-use
Model / Ref / Catalog
Single-use FillerCollector, 250ml, Collect Fat, 1660000-5
Primary DI / UDI-DI
04260170881083
FDA product code
QKL
GMDN term
Surgical suction system collection container, single-use
Device class
Class II
Regulation number
878.5040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical suction system collection container, single-use

Similar devices in this category

Other devices filed under Surgical suction system collection container, single-use.

Other devices from Human Med AG

See all devices from Human Med AG →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (9, all answered No)