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Teleport Microcatheter - EUDAMED Registration 06934955943010

Access comprehensive regulatory information for Teleport Microcatheter in the European Union medical device market through Pure Global AI's free database. This Class III device is registered with EU EUDAMED under Primary DI 06934955943010 and manufactured by OrbusNeich Medical (Shenzhen) Co.,Ltd in China.

This page provides complete registration details including trade name (Teleport Microcatheter), manufacturer information, authorized representative details, competent authority (Health Board, Medical Devices Department), 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 III
06934955943010
No
Teleport Microcatheter
Trade Name: Teleport Microcatheter
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Device Description (EMDN)

PHARMACEUTICAL INFUSION AND ADMINISTRATION INTRAVASCULAR CATHETERS AND MICROCATHETERS

Device Classification
Risk Class
Class III
CND Nomenclatures Code
C0104020205
Trade Name
Teleport Microcatheter
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06934955943010
Basic UDI
B-06934955943010
Version Date
July 18, 2023
Manufacturer Last Update
May 16, 2022
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
1 Jinkui Road People's Republic of China
Email
onra@orbusneich.com
Authorized Representative
SRN
EE-AR-000004308
Country
Estonia
Address
30 Laki tn Tallinn
Email
enquiries@qualityfirstint.com
Telephone
+3726104196
Regulatory Information
Competent Authority
Health Board, Medical Devices Department
Applicable Legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed On The Market
Italy
Market Available
Italy:2021-01-19~None
Device Characteristics
Human Tissues
No
Animal Tissues
No