INTER MEDICAL MEDIZINTECHNIK GMBH

FDA Device Registration & Listing · LUEBBECKE North Rhine-Westphalia, DE · Registration 3006611212

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
3006611212
FEI Number
3006611212
Entity Name
INTER MEDICAL MEDIZINTECHNIK GMBH
City/State/Country
LUEBBECKE North Rhine-Westphalia, DE
Establishment Address
DAIMLERSTRASSE 34-36, LUEBBECKE North Rhine-Westphalia D-32312, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
INTER MEDICAL MEDIZINTECHNIK GMBH (Owner Number: 9077300)
Owner / Operator Contact Address
DAIMLERSTRASSE 34-36, --, LUEBBECKE, DE-NW D-32312, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MultiCam 3000

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPS System, Tomography, Computed, Emission Radiology Class 2 892.1200 2020-02-03

Official Correspondent

HANS GUENTER OSIEK

US Agent Details

John Shaw Email: jshaw.northeastnme@gmail.com Phone: (603) 4907404

Related Public Records

Same Entity

INTER MEDICAL MEDIZINTECHNIK GMBH
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
K033956 Is2 Research, Inc. MOBILE SINGLE CIRCULAR CAMERA (MSC) & MOBILE DIGITAL CARDIAC CAMERA (MDCC) 2004-01-20
K923309 GE Medical Systems ARGUS PET SYSTEM 1992-09-29
K101768 Miegmbh MIE SCINTRON GAMMA CAMERA SYSTEMS 2010-10-05

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0005-2016 Toshiba American Medical Systems Inc 2
Celesteion PCA-9000A/2 PET/CT System
Z-0012-05 General Electric Med Systems LLC 2
Emission Computed Tomography System. Including Model numbers: 2200967, ASM001080, ASM001083, ASM001092, ASM001099, ASM000085, 10036800109, and Varicam.
Z-0013-2007 Philips Medical Systems (Cleveland) Inc 2
Nuclear medicine systems: Gemini 16, Model 4535 679 28961. Gemini GXL, Models # 4535 679 71891, #4535 679 75681, #4535 679 75691. Precedence, Model #2169 -3000A, #2169-3001A, #2169-3002A, and 2169-3003A. PET/CT Computed tomography systems.
Z-0014-2007 Philips Medical Systems (Cleveland) Inc 2
Brilliance(a) CT 6 slice, Model #4535 670 73191. Brilliance(a) CT 10 Slice, Model 4535 670 73181. Brilliance 16 Slice, Model #4535 670 78851. Brilliance CT 16 Power, Model #4535 670 23331. Brilliance CT 40 Slice, Model #4550 110 04011. Brilliance CT Big Bore, Model #4535 670 88051. Computed tomography systems.
Z-0024-2014 GE Healthcare, LLC 2
GE PET Discovery 610, PET Discovery 710. Intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006611212. Last updated year: 2026. Please use registration number 3006611212 when referencing this establishment in official correspondence.
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