Skip to content

CryoPRO™-5 SGI-0442

by Thermogenesis Corp.

CryoPRO™-5 SGI-0442 is a Class II device made by Thermogenesis Corp., listed in FDA GUDID since 24 Sep 2016 (UDI-DI B039SGI04420), 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 NumberB039SGI04420 UDI-DI Date24 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  • Withdrawn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

Trade name
CryoPRO™-5
Generic name
Blood cell freeze/thaw system
Model / reference
SGI-0442
Primary DI / UDI-DI
B039SGI04420
FDA product code
OAO
GMDN term
Blood cell freeze/thaw system
Device class
Class II
Regulation number
864.9900
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood cell freeze/thaw system

Other devices from Thermogenesis Corp.

See all devices from Thermogenesis Corp. →

Properties

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