PETER BUESCHER GMBH

FDA Device Registration & Listing · Bergisch Gladbach North Rhine-Westphalia, DE · Registration 3015540002

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
3015540002
FEI Number
3015540002
Entity Name
PETER BUESCHER GMBH
City/State/Country
Bergisch Gladbach North Rhine-Westphalia, DE
Establishment Address
Vuerfelser Kaule 1, Bergisch Gladbach North Rhine-Westphalia 51427, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Peter Buescher GmbH (Owner Number: 10060878)
Owner / Operator Contact Address
Vuerfelser Kaule 1, Bergisch Gladbach, DE-NW 51427, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAC Dressing, Wound, Hydrophilic General, Plastic Surgery Class 1 878.4018 2020-10-27

Official Correspondent

Marc Schmalfeldt

US Agent Details

Jason Woehrle Business: COLOPLAST CORP. Email: usjawo@coloplast.com Phone: (612) 7302063

Related Public Records

Same Entity

Peter Buescher 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 3015540002. Last updated year: 2026. Please use registration number 3015540002 when referencing this establishment in official correspondence.
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