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MXP Device 8-5139

by Thermogenesis Corp.

MXP Device 8-5139 is a Class I device made by Thermogenesis Corp., listed in FDA GUDID since 5 Apr 2017 (UDI-DI 00886368000353), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00886368000353 UDI-DI Date5 Apr 2017ListedStatusListed 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  • Withdrawn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
MXP Device
Generic name
Haematological concentrate system preparation kit, bone marrow concentration
Model / Ref / Catalog
8-5139
Primary DI / UDI-DI
00886368000353
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, bone marrow concentration

Similar devices

Other devices filed under FDA product code JQC (Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use).

Other devices from Thermogenesis Corp.

See all devices from Thermogenesis Corp. →

Properties

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