SANMINA-SCI AB

FDA Device Registration & Listing · SJALEVAD Vasternorrland, SE · Registration 3004201275

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
3004201275
FEI Number
3004201275
Entity Name
SANMINA-SCI AB
City/State/Country
SJALEVAD Vasternorrland, SE
Establishment Address
SVEDJEVAGEN 12, SJALEVAD Vasternorrland 89435, SE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Sanmina Corporation (Owner Number: 2129538)
Owner / Operator Contact Address
13000 S. Memorial Pkwy, --, Huntsville, AL 35803, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Afinion™ 2 analyzer COMPODOCK

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JQT Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica Clinical Chemistry Class 1 862.2400 2018-04-06
KSB Set, Transfer (Blood/Plasma) Hematology Class 2 864.9875 2007-12-05

Official Correspondent

No official correspondent registered.

US Agent Details

Jeffrey Stahl Business: Sanmina Email: jeffrey.stahl@sanmina.com Phone: (256) 4794797

Related Public Records

Same Entity

Sanmina 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
3004139819 Sanmina Ireland UC FERMOY, CORK Munster, IE
3009609218 Sanmina Corporation Carrollton, TX, US
3007867838 Sanmina SAN JOSE, CA, US
3004016520 SANMINA- SCI ISRAEL MEDICAL SYSTEMS LTD. Maalot-Tarshiha Northern, IL
3007923088 Sanmina-SCI Systems (Malaysia) Sdn Bhd Perai Pulau Pinang, MY

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K915332 Ciba Corning Diagnostics Corp. MODEL 795 FLUOROMETER/DENSITOMETER 1992-02-18

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004201275. Last updated year: 2026. Please use registration number 3004201275 when referencing this establishment in official correspondence.
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