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Multi-Link™ 2090101-611

by Carefusion Finland 320 Oy

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10190752100206 UDI-DI Date11 Jul 2017ListedStatusListed GUDID: not in commercial distribution

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  • Withdrawn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, single-use
Model / Ref / Catalog
2090101-611
Primary DI / UDI-DI
10190752100206
FDA Product Code
DSA
GMDN Term
Electrocardiographic lead set, single-use
Device Class
Class II
Regulation Number
870.2900
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Unsafe

Properties

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

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No