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Vista ®

FDA UDI

Class II (US FDA UDI)

by Terumo BCT, Inc..

Identity

Trade Name
Vista ® FDA UDI
Generic Name
Blood bank information system FDA UDI
Device Name
Vista® Information System Version 4 Vista Standard Interface and SafeTrace® BBSI Installation Guide FDA UDI
Model / Reference
25203 FDA UDI
Description
Vista® Information System Version 4 Vista Standard Interface and SafeTrace® BBSI Installation Guide FDA UDI

Identifiers

Primary DI / UDI-DI
05020583252035 FDA UDI
FDA Product Code
MMH FDA UDI
GMDN Term
Blood bank information system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9165 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood bank information system

Vista ® by Terumo BCT, Inc.. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood bank information system.

Cleared under the same submission

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 45e46c01-e4c1-4458-8c04-af7827cb4886 36 fields · synced Jun 6, 2026