Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011676349

FEI Number

3011676349

Entity Name

TIGRIS ELEKTRONIK GMBH

City/State/Country

Berlin, DE

Establishment Address

Teltowkanalstrasse 2, Berlin 12247, DE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

TIGRIS Elektronik GmbH (Owner Number: 10049154)

Owner / Operator Contact Address

Teltowkanalstrasse 2, Berlin, DE-BE 12247, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

WA97020A, Light source, LED WA97020A, Light source, LED WA97010A, Light source, for stroboscopy Light Source for Stroboscopy WA97010A

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FCW	Light Source, Fiberoptic, Routine	Gastroenterology, Urology	Class 2	876.1500	2019-12-17
NTN	Led Light Source	Gastroenterology, Urology	Class 2	876.1500	2019-12-17
EQH	Source, Carrier, Fiberoptic Light	Ear, Nose, Throat	Class 1	874.4350	2019-12-17
EQL	Laryngostroboscope	Ear, Nose, Throat	Class 1	874.4750	2023-07-19

Official Correspondent

Guido Kuhlmann

US Agent Details

German American Chamber of Commerce, Inc. German American Ch Email: legalservices@gaccny.com Phone: (212) 9748830

Related Public Records

Same Entity

TIGRIS Elektronik 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 3011676349. Last updated year: 2026. Please use registration number 3011676349 when referencing this establishment in official correspondence.