Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006776693

FEI Number

3006776693

Entity Name

Diagramma AG

City/State/Country

Dietikon Zurich, CH

Establishment Address

Zuercherstrasse 152, Dietikon Zurich 8953, CH

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Diagramma Dietikon AG (Owner Number: 10023763)

Owner / Operator Contact Address

Zuercherstrasse 152, Dietikon, CH-ZH 8953, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CTG paper ECG paper EEG / EMG paper

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DSF	Recorder, Paper Chart	Cardiovascular	Class 1	870.2810	2007-12-13

Official Correspondent

Pascal Treyer

US Agent Details

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

Related Public Records

Same Entity

Diagramma Dietikon AG

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K770946	Instrumentation Laboratory CO	RECORD, MODEL 702, I.L.	1977-07-05

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3032916632	BECTON, DICKINSON AND COMPANY	Irvine, CA, US
3016701404	Philips North America LLC	Export, PA, US
3008729547	GE Medical Systems Information Technologies - Critikon de Mexico S. de R.L. de C.V.	JUAREZ Chihuahua, MX

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006776693. Last updated year: 2026. Please use registration number 3006776693 when referencing this establishment in official correspondence.