ENGLERT GMBH & CO. KG

FDA Device Registration & Listing · Wertheim Baden-Wurttemberg, DE · Registration 3012309966

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
3012309966
FEI Number
3012309966
Entity Name
ENGLERT GMBH & CO. KG
City/State/Country
Wertheim Baden-Wurttemberg, DE
Establishment Address
Obere Grueben 11, Wertheim Baden-Wurttemberg 97877, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Englert GmbH & Co. KG (Owner Number: 10084660)
Owner / Operator Contact Address
Obere Grueben 11, Wertheim, DE-BW 97877, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

V-707377 USS Module Calibration Syringe 1/3 Liter

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BXP Transducer, Gas Flow Anesthesiology Class 1 868.2885 2022-04-21
BXW Calibrator, Volume, Gas Anesthesiology Class 1 868.1870 2022-03-18

Official Correspondent

Richard Ries

US Agent Details

Emily Matorin Business: Pragmatic Compliance dba FDAbasics Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

Englert GmbH & Co. KG
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 3012309966. Last updated year: 2026. Please use registration number 3012309966 when referencing this establishment in official correspondence.
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