SARSTEDT APS

FDA Device Registration & Listing · Bording Midtjylland, DK · Registration 3020703807

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
3020703807
FEI Number
3020703807
Entity Name
SARSTEDT APS
City/State/Country
Bording Midtjylland, DK
Establishment Address
Brogesvej 18, Bording Midtjylland 7441, DK
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
SARSTEDT ApS (Owner Number: 10082841)
Owner / Operator Contact Address
Brogesvej 18, Bording, DK-82 7441, DK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use Clinical Chemistry Class 1 862.2050 2021-10-07

Official Correspondent

Keld Joergensen

US Agent Details

Susan Smith Business: SARSTEDT, INC. Email: susan.smith@sarstedt.com Phone: (828) 4654000

Related Public Records

Same Entity

SARSTEDT ApS
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2008 Beckman Coulter Inc 1
FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013 Biomerieux Inc 1
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020703807. Last updated year: 2026. Please use registration number 3020703807 when referencing this establishment in official correspondence.
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