10 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Country: Ireland
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RespiraSense
Device
EU MDD
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Eu Md Class 2b
·PMD Device Solutions Ltd·On the market·1 country
RespiraSense App
Device
EU MDR
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Eu Md Class 2a
·PMD Device Solutions Ltd·On the market·1 country
RespiraSense
Device
EU MDR
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Eu Md Class 2a
·PMD Device Solutions Ltd·On the market·1 country
RespiraSense
Device
EU MDR
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Eu Md Class 2a
·PMD Device Solutions Ltd·On the market·1 country
RespiraSense
Device
EU MDR
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Eu Md Class 2a
·PMD Device Solutions Ltd·On the market·1 country
RespiraSense patient respiratory monitor system
Basic UDI-DI
EU MDD
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Eu Md Class 2b
·PMD Device Solutions Ltd·1 device
RespiraSense patient respiratory monitor system.
Basic UDI-DI
EU MDR
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Eu Md Class 2a
·PMD Device Solutions Ltd·4 devices
SEROLOGY ToRCH lgM 2022 POSITIVE CONTROLI Intended for use with in vitro assays for determination of IgM antibodies to Cytomegalovirus (CMV), IgM antibodies to Rubella Virus, IgM antibodies to Toxoplasma gondii, IgM antibodies to Herpes Simplex Virus Type 1 and 2. Catalog Number: SR10349
FDA Enforcement
Class III
·Ongoing·Randox Laboratories Ltd.·January 10, 2024
GB19/964252
Certificate
MDD Annex II (excluding section 4)·PMD Device Solutions Ltd·SGS Belgium NV·1 Basic UDI-DI
D P Medical Systems (Ireland) Limited
Importer
🇮🇪 Ireland·6 Manufacturers