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Multi-Sampling Connector 4R5129

by Fresenius Kabi

Multi-Sampling Connector 4R5129 is a Class I device made by Fresenius Kabi, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 04086000101240), 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 Number04086000101240 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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-Sampling Connector
Generic name
Luer-ended blood collection tube spike
Model / Ref / Catalog
4R5129
Primary DI / UDI-DI
04086000101240
FDA product code
KST
GMDN term
Luer-ended blood collection tube spike
Device class
Class I
Regulation number
864.9125
GUDID distribution status
In Commercial Distribution

Related devices

Category: Luer-ended blood collection tube spike

Similar devices in this category

Other devices filed under Luer-ended blood collection tube spike.

Other devices from Fresenius Kabi

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Properties

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