TESCOM EUROPE GmbH & CO. KG

FDA Device Registration & Listing · Selmsdorf Mecklenburg-Western Pomerania, DE · Registration 3004859326

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
3004859326
FEI Number
3004859326
Entity Name
TESCOM EUROPE GmbH & CO. KG
City/State/Country
Selmsdorf Mecklenburg-Western Pomerania, DE
Establishment Address
An der Trave 23-25, Selmsdorf Mecklenburg-Western Pomerania 23923, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
TESCOM EUROPE GMBH CO KG (Owner Number: 10044413)
Owner / Operator Contact Address
An der Trave 23-25, Selmsdorf, DE-MV 23923, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TESCOM Pressure Regulator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAN Regulator, Pressure, Gas Cylinder Anesthesiology Class 1 868.2700 2013-06-07

Official Correspondent

No official correspondent registered.

US Agent Details

Brian Tutt Business: Global Director of Engineering Email: brian.tutt@emerson.com Phone: (763) 2413345

Related Public Records

Same Entity

TESCOM EUROPE GMBH CO KG
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-0037-2010 Airgas Puritan Medical Puritan Medical Unit 1
AGI-2237 Portable 2 Cylinder Manifold Cart, for connecting medical gas cylinders.
Z-0038-2010 Airgas Puritan Medical Puritan Medical Unit 1
AGI-2238 Portable 4 Cylinder Manifold Cart, for connecting medical gas cylinders.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004859326. Last updated year: 2026. Please use registration number 3004859326 when referencing this establishment in official correspondence.
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