ELM-PLASTIC GMBH

FDA Device Registration & Listing · Dudeldorf Rhineland-Palatinate, DE · Registration 3008801173

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
3008801173
FEI Number
3008801173
Entity Name
ELM-PLASTIC GMBH
City/State/Country
Dudeldorf Rhineland-Palatinate, DE
Establishment Address
Kollenbergstrasse 7, Dudeldorf Rhineland-Palatinate 54647, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
elm-plastic GmbH (Owner Number: 10045574)
Owner / Operator Contact Address
Kollenbergstrasse 7, Dudeldorf, DE-RP 54647, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Plastic dosing pipette

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2013-12-03

Official Correspondent

Sascha Moehs

US Agent Details

Larry Ordet Business: FDA Solutions Group LLC Email: info@fdasolutionsgroup.com Phone: (305) 7023161

Related Public Records

Same Entity

elm-plastic GmbH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008801173. Last updated year: 2026. Please use registration number 3008801173 when referencing this establishment in official correspondence.
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