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Magellan MAR0Max Convenience kit

by Arteriocyte Medical Systems, Inc

Magellan MAR0Max Convenience kit is a Class I device made by Arteriocyte Medical Systems, Inc, listed in FDA GUDID since 9 Sep 2016 (UDI-DI M896MAR0MAX0), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM896MAR0MAX0 UDI-DI Date9 Sep 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic name
Haematological concentrate system preparation kit, bone marrow concentration
Model / Ref / Catalog
MAR0Max
Primary DI / UDI-DI
M896MAR0MAX0
FDA product code
JQC
GMDN term
Haematological concentrate system preparation kit, bone marrow concentration
Device class
Class I
Regulation number
862.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Haematological concentrate system preparation kit, platelet concentration

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Properties

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