Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022040661

FEI Number

3022040661

Entity Name

COMPREMIUM AG

City/State/Country

Muri Bern, CH

Establishment Address

Worbststrasse 46, Muri Bern 3074, CH

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Compremium AG (Owner Number: 10090973)

Owner / Operator Contact Address

Worbststrasse 46, Muri, CH-BE 3074, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K223509

PMA Number

N/A

All Registered Proprietary Names

CPMX1 Compremium Quantis ST

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LXC	Monitor, Pressure, Intracompartmental	Unknown	Class U	N/A	2024-06-10

Official Correspondent

Vincent Baumann

US Agent Details

Doug Dockhorn Business: Veranex Inc. Email: usagent@veranex.com Phone: (919) 8276653

Related Public Records

Same Entity

Compremium AG

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0034-06	Stryker Instruments Div. of Stryker Corporation	U	Stryker brand Intra-Compartmental (STIC) Pressure Monitor, Model 295-001-000.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022040661. Last updated year: 2026. Please use registration number 3022040661 when referencing this establishment in official correspondence.