Skip to content

Trima Accel 82656

by Terumo BCT, Inc.

Trima Accel 82656 is a blood transfer set (FDA Class II; FDA product code GKT, Separator, automated, blood cell, diagnostic) made by Terumo BCT, Inc., listed in FDA GUDID since 15 Feb 2017 (UDI-DI 05020583826564), 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 Number05020583826564 UDI-DI Date15 Feb 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  • Withdrawn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
Trima Accel
Generic name
Blood transfer set
Model / reference
82656
Primary DI / UDI-DI
05020583826564
FDA product code
GKT
GMDN term
Blood transfer set
Device class
Class II
Regulation number
864.9245
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 Terumo BCT, Inc.

See all devices from Terumo BCT, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)