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Rem Systems B 898

by CODAN US Corporation

Rem Systems B 898 is a blood transfer set (FDA Class II; FDA product code FPA, Set, Administration, Intravascular) made by CODAN US Corporation, listed in FDA GUDID since 30 Apr 2021 (UDI-DI 10897891001585), 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 Number10897891001585 UDI-DI Date30 Apr 2021ListedStatusListed 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  • Withdrawn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
Rem Systems
Generic name
Blood transfer set
Model / reference
B 898
Primary DI / UDI-DI
10897891001585
FDA product code
FPA
GMDN term
Blood transfer set
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood transfer set

Similar devices in this category

Other devices filed under Blood transfer set.

Other devices from CODAN US Corporation

See all devices from CODAN US Corporation →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)