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Blood Product Questionnaire Module

FDA UDI

Class II (US FDA UDI)

by Buoy Software Llc

Identity

Trade Name
Blood Product Questionnaire Module FDA UDI
Generic Name
Blood bank information system application software FDA UDI
Device Name
The Blood Product Questionnaire Module supports single and/or multi-site blood establishment collection facilities’ creation of a donor history questionnaire, the collection of donor history by donors, the determination of visit requirements, and the determination of donor eligibility through system logic or via analysis by trained facility staff members FDA UDI
Model / Reference
1 FDA UDI
Description
The Blood Product Questionnaire Module supports single and/or multi-site blood establishment collection facilities’ creation of a donor history questionnaire, the collection of donor history by donors, the determination of visit requirements, and the determination of donor eligibility through system logic or via analysis by trained facility staff members FDA UDI

Identifiers

Primary DI / UDI-DI
00860010651209 FDA UDI
FDA Product Code
MMH FDA UDI
GMDN Term
Blood bank information system application software 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood bank information system application software

Blood Product Questionnaire Module by Buoy Software Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood bank information system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Buoy Software Llc

Sources (1)

  • FDA UDI 718324f9-9dae-4226-b345-002f7744323e 34 fields · synced Jun 8, 2026