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Multi-Link™ 411202-002

by AirLife Finland Oy

Multi-Link 411202-002 is an electrocardiographic lead set (FDA Class II; FDA product code DSA, Cable, Transducer And Electrode, Patient, (Including Connector)) made by AirLife Finland Oy, listed in FDA GUDID since 23 Nov 2018 (UDI-DI 10190752106598), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10190752106598 UDI-DI Date23 Nov 2018ListedStatusListed 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  • Withdrawn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

Trade name
Multi-Link™
Generic name
Electrocardiographic lead set, reusable
Model / Ref / Catalog
411202-002
Primary DI / UDI-DI
10190752106598
FDA product code
DSA
GMDN term
Electrocardiographic lead set, reusable
Device class
Class II
Regulation number
870.2900
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Electrocardiographic lead set, reusable

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Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)