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Trima Accel®

FDA UDI

Class II (US FDA UDI)

by Terumo BCT, Inc..

Identity

Trade Name
Trima Accel® FDA UDI
Generic Name
Blood transfer set FDA UDI
Device Name
Disposable Tubing Sets, RBC, Plasma Set FDA UDI
Model / Reference
80500 FDA UDI
Description
Disposable Tubing Sets, RBC, Plasma Set FDA UDI

Identifiers

Primary DI / UDI-DI
05020583805002 FDA UDI
FDA Product Code
GKT FDA UDI
GMDN Term
Blood transfer set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9245 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood transfer set

Trima Accelé offers a disposable blood transfer set for hematological procedures, designed to provide quick and convenient access to lab-grown red blood cells and plasma. With its proprietary storage conditions and sterilization process, this device ensures the safe handling of sensitive medical products.

Similar devices

Also classified as Blood transfer set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terumo BCT, Inc..

Sources (1)

  • FDA UDI 2769d9dc-751a-459d-8647-e0c0a94cd36a 35 fields · synced Jul 4, 2026