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Donor Doc

FDA UDI

Class II (US FDA UDI)

by Haemonetics Corporation

Identity

Trade Name
Donor Doc FDA UDI
Generic Name
Configurable electronic form web-based application software FDA UDI
Device Name
Donor Doc version 3.x.x FDA UDI
Model / Reference
3.x.x FDA UDI
Description
Donor Doc version 3.x.x FDA UDI

Identifiers

Primary DI / UDI-DI
00812747010200 FDA UDI
FDA Product Code
MMH FDA UDI
GMDN Term
Configurable electronic form web-based 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Configurable electronic form web-based application software

Donor Doc by Haemonetics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Configurable electronic form web-based application software.

Cleared under the same submission

BK140183 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 02d3151a-12ce-422a-beae-b2ca2d292ef6 35 fields · synced Jun 8, 2026