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Extraction cannula

by Human Med AG

Extraction cannula (675010-5) is a Class II device made by Human Med AG, listed in FDA GUDID since 30 Jul 2025 (UDI-DI 04260170881441), registry data as of 21 Oct 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 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04260170881441 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  • Withdrawn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
Collection syringe adaptor, single-use
Model / Ref / Catalog
Extraction cannula, sterile/SU, Luer connector, 675010-5
Primary DI / UDI-DI
04260170881441
FDA product code
QKL
GMDN term
Collection syringe adaptor, single-use
Device class
Class II
Regulation number
878.5040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Collection syringe adaptor, single-use

Similar devices

Other devices filed under FDA product code QKL (Lipoaspirate Washing System For Aesthetic Body Contouring).

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)