Sartorius Liquid Handling Oy

FDA Device Registration & Listing · Kajaani, Finland Kainuu, FI · Registration 3010127792

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
3010127792
FEI Number
3010127792
Entity Name
Sartorius Liquid Handling Oy
City/State/Country
Kajaani, Finland Kainuu, FI
Establishment Address
Tietokatu 4, Kajaani, Finland Kainuu 87400, FI
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Sartorius Stedim North America Inc./Sartorius Corporation (Owner Number: 9005426)
Owner / Operator Contact Address
545-1 Johnson Ave, Bohemia, NY 11716, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Proline Plus 8-ch (728120, 728130, 728140) Optifit Tips 10 ml (LH-799000, LH-799004) Mline 12-ch (725220, 725230, 725240) Optifit Tips 1200 µl (791200, 791201, 791202, 791203, 791210, 791210, 791211, 791212, 791213, LH-B791204, LH-EB791204) Optifit Tips 5 mL (780300, 780304, 780305, 780308) Optifit Tips 1000 µl (791000, 791001, 791002, 791003, 791020, 791021, LH-B791004, LH-B791024, LH-EB791004, LH-X791000, L Picus2 12-ch (LH-747041, LH-747061, LH-747421, LH-747491) Safetyspace Filter Tip 120 µl (790101F) Optifit Tips 200 µl (790200, 790201, 790202, 790203, LH-B790204, LH-EB790204) Mline 1-ch (725010, 725020, 725030, 725050, 725060, 725070, 725080, 725090) Optifit Tips 350 µl (790350, 790351, 790352, 790353, LH-B790354, LH-EB790354) Picus2 8-ch (LH-747321, LH-747341, LH-747361, LH-747391) Picus2 1-ch (LH-747021, LH-747041, LH-747061, LH-747081, LH-747101, LH-747111) Proline Plus 12-ch (728220, 728230, 728240) Proline Plus 1-ch (728010, 728020, 728030, 728050, 728060, 728070, 728080, 728090, 728515, 728520, 728530, 728535, Mline 8-ch (725120, 725130, 725140) Safetyspace Filter Tip 300 µl (790301F) Safetyspace Filter Tip 20 µl (790021F) Optifit Tips 10 µl (790010, 790011, 790012, 790013, 790014) Safetyspace Filter Tip 200 µl (790201F) Safetyspace Filter Tip 1200 µl (791211F) Safetyspace Filter Tip 1000 µl (791001F) Safetyspace Filter Tip 10 µl (790011F) Safetyspace Filter Tip 5 mL (LH-795001F) Proline Plus 1-ch 728545, 728550, 728560, 728565, 728567, 728570, 728575, 728580, 728590)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JRC Micro Pipette Clinical Chemistry Class 1 862.2050 2013-01-16

Official Correspondent

Terri Brooks

US Agent Details

Terri Brooks Business: Sartorius Stedim North America Email: terri.brooks@sartorius.com Phone: (631) 4699877

Related Public Records

Same Entity

Sartorius Stedim North America Inc./Sartorius Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3007699074 Sartorius Stedim Lab Ltd. Stonehouse Gloucestershire, GB

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010127792. Last updated year: 2026. Please use registration number 3010127792 when referencing this establishment in official correspondence.
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