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Adhesive specimen microscopy slide (IVD) - EUDAMED Registration 04064279018315

Access comprehensive regulatory information for Adhesive specimen microscopy slide (IVD) in the European Union medical device market through Pure Global AI's free database. This Class A device is registered with EU EUDAMED under Primary DI 04064279018315 and manufactured by Paul Marienfeld GmbH & Co. KG in Germany.

This page provides complete registration details including trade name (Histobond+ weiรŸ Eck 2 versetzte Ringe V=100 Plasch Tharmac), manufacturer information, competent authority (DE/CA37, Regierungsprรคsidium Stuttgart), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.

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EUDAMED Official Data
Class A
04064279018315
No
Adhesive specimen microscopy slide (IVD)
Trade Name: Histobond+ weiรŸ Eck 2 versetzte Ringe V=100 Plasch Tharmac
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Device Description (EMDN)

MICROSCOPE SLIDES

Device Classification
Risk Class
Class A
CND Nomenclatures Code
W0503900201
Trade Name
Histobond+ weiรŸ Eck 2 versetzte Ringe V=100 Plasch Tharmac
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
04064279018315
Basic UDI
4250317304OTHBU4
Version Date
December 05, 2024
Manufacturer Last Update
May 11, 2022
Active Status
No
Manufacturer
Country
Germany
Country Type
EU_MEMBER_STATE
Address
4 Am Wรถllerspfad Lauda-Kรถnigshofen
Email
info@marienfeld-superior.com
Regulatory Information
Competent Authority
DE/CA37, Regierungsprรคsidium Stuttgart
Applicable Legislation
IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
Placed On The Market
Germany
Device Characteristics
Human Tissues
No
Animal Tissues
No