BioLife Plasma Services L.P.

FDA Device Registration & Listing · Bannockburn, IL, US · Registration 3016429887

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3016429887
FEI Number
3016429887
Entity Name
BioLife Plasma Services L.P.
City/State/Country
Bannockburn, IL, US
Establishment Address
1200 Lakeside Drive, Bannockburn, IL 60015, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
BioLife Plasma Services L.P. (Owner Number: 9029757)
Owner / Operator Contact Address
1200 Lakeside Drive, Bannockburn, IL 60015, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
BK241136
PMA Number
N/A

All Registered Proprietary Names

Automated Plasma Dispositioning System (APDS) v2 Lookback Notification System (LNS) version 2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMH Blood Establishment Computer Software And Accessories Hematology Class 2 864.9165 2017-01-23
MMH Blood Establishment Computer Software And Accessories Hematology Class 2 864.9165 2025-09-22

Official Correspondent

Jennifer Burton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BioLife Plasma Services L.P.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016429887. Last updated year: 2026. Please use registration number 3016429887 when referencing this establishment in official correspondence.
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