10,000 results
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20ms
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Sources: EU EUDAMED, US FDA
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Country: Germany
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JaviTech e.K.
Authorized representative
🇩🇪 Germany·111 Manufacturers·1816 Devices
Jason M44s
Device
EU MDR
·
Eu Md Class 1
·ellen wille THE HAIR-COMPANY GmbH·On the market·31 countries
K3Pro Titanium base
Device
EU MDD
·
Eu Md Class 2b
·Argon Medical Production & Vertriebs Gesellschaft mbH & Co. KG·On the market·8 countries
Stimulation Tube
Device
EU MDD
·
Eu Md Class 1
·Joimax GmbH·On the market·19 countries
VITAPAN PLUS®
Device
EU MDD
·
Eu Md Class 2a
·VITA Zahnfabrik·No longer on the market·1 country
VITAPAN PLUS®
Device
EU MDD
·
Eu Md Class 2a
·VITA Zahnfabrik·No longer on the market·1 country
natural 4.0 Li
Device
EU MDR
·
Eu Md Class 2a
·audifon GmbH & Co. KG·Not intended for eu market
LiMAx breathing mask
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·Humedics GmbH·1 device
LiMAx device
Basic UDI-DI
EU MDD
·
Eu Md Class 2b
·Humedics GmbH·1 device
human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107, sterile, single use.
FDA Enforcement
Class II
·Ongoing·HUMAN MED AG·March 12, 2025
DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)
FDA Enforcement
Class II
·Ongoing·Pro-Med Instruments Gmbh·June 4, 2025
pmi, pro med instruments, DORO(R) Sterile Disposable Skull Pins, 3 pieces (3 pieces per blister, 12 blisters per box), STERILE R, Rx ONLY The DORO(R) Skull Pins are inserted into the receptacles of the skull clamp and fixate the head during surgery.
FDA Enforcement
Class II
·Terminated·Pro-Med Instruments Gmbh·December 13, 2017
DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries
FDA Enforcement
Class I
·Terminated·Pro-Med Instruments Gmbh·September 26, 2018
DORO LUCENT Locking Transitional Member, REF 1101.031 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries
FDA Enforcement
Class I
·Terminated·Pro-Med Instruments Gmbh·September 26, 2018
DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries
FDA Enforcement
Class I
·Terminated·Pro-Med Instruments Gmbh·September 26, 2018
GfM mbH
System producer
🇩🇪 Germany
Bürki inno med GmbH
Importer
🇩🇪 Germany·1 Manufacturer
DD601424180001
Certificate
MDD Annex V·RECA Med GmbH·TÜV Rheinland LGA Products GmbH·2 Basic UDI-DIs
DD 601424180001
Certificate
MDD Annex V·RECA Med GmbH·TÜV Rheinland LGA Products GmbH·1 Basic UDI-DI
AirLife Medizintechnik
Importer
🇩🇪 Germany·2 Manufacturers