KABE LABORTECHNIK GMBH

FDA Device Registration & Listing · NUMBRECHT North Rhine-Westphalia, DE · Registration 8010932

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
8010932
FEI Number
3002807393
Entity Name
KABE LABORTECHNIK GMBH
City/State/Country
NUMBRECHT North Rhine-Westphalia, DE
Establishment Address
JAGERHOFSTR. 17, NUMBRECHT North Rhine-Westphalia 51588, DE
Establishment Type(s)
Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
KABE LABORTECHNIK GMBH (Owner Number: 8010932)
Owner / Operator Contact Address
JAGERHOFSTR. 17, --, NUMBRECHT, DE-NOTA 51588, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SAFE-T-FILL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GIO Tube, Collection, Capillary Blood Hematology Class 1 864.6150 2001-10-22

Official Correspondent

Diana Rogers

US Agent Details

Diana Rogers Business: ASP Global Email: diana.rogers@aspglobal.com Phone: (404) 6966999

Related Public Records

Same Entity

KABE LABORTECHNIK GMBH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3015908492 VETIRUS, LLC Naples, FL, US
1000555938 SC-SANGUIS COUNTING GMBH NUEMBRECHT North Rhine-Westphalia, DE
9610126 ROCHE DIAGNOSTICS GMBH MANNHEIM Baden-Wurttemberg, DE
3005739529 Zhejiang Gongdong Medical Technology Co., Ltd TAIZHOU Zhejiang, CN
1064584 DEMETECH CORP. Miami Lakes, FL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8010932. Last updated year: 2026. Please use registration number 8010932 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.