FDA Device Registration & Listing · Willstatt Baden-Wurttemberg, DE · Registration 3043616309
Public RecordDevice ListingExpiry 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
3043616309
FEI Number
3043616309
Entity Name
PHILIPP KIRSCH GMBH
City/State/Country
Willstatt Baden-Wurttemberg,
DE
Establishment Address
Im Lossenfeld 14, Willstatt Baden-Wurttemberg 77731, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Philipp Kirsch GmbH (Owner Number: 10095114)
Owner / Operator Contact Address
Im Lossenfeld 14, Willstätt, DE-BW 77731, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A
All Registered Proprietary Names
BL 300 US PRO-ACTIVEFROSTER BL 530 US ULTIMATEBL 340 US PRO-ACTIVEFROSTER BL 730 US ULTIMATEFROSTER BL 530 US PRO-ACTIVEBL 340 US ULTIMATEFROSTER BL 330 US ULTIMATEBL 100 US PRO-ACTIVEFROSTER BL 730 US PRO-ACTIVEBL 520 US PRO-ACTIVEBL 720 US PRO-ACTIVEBL 300 US ULTIMTAEBL 720 US ULTIMATEBL 520 US ULTIMATEFROSTER BL 330 US PRO-ACTIVE
Source Citation & Summary:
This public preview is extracted from openFDA device registration and listing logs under registration number 3043616309.
Last updated year: 2026.
Please use registration number 3043616309 when referencing this establishment in official correspondence.
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