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Quill PDO - EUDAMED Registration 00848782019144

Access comprehensive regulatory information for Quill PDO 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 00848782019144 and manufactured by Surgical Specialties Mexico S. DE R.L. DE C.V. in Mexico.

This page provides complete registration details including trade name (Quill PDO), manufacturer information, authorized representative details, competent authority (DE/CA39, Regierungsprรคsidium Freiburg Referat 25), 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
00848782019144
No
Quill PDO
Trade Name: Quill PDO
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Device Description (EMDN)

POLYDIOXANONE MONOFILAMENT WITH NEEDLE FOR OPEN SURGERY

Device Classification
Risk Class
Class III
CND Nomenclatures Code
H010101010101
Trade Name
Quill PDO
Implantable
Yes
Reusable
No
Measuring Function
No
Registration Information
Primary DI
00848782019144
Basic UDI
B-00848782019144
Version Date
July 02, 2024
Manufacturer Last Update
June 11, 2024
Active Status
No
Manufacturer
Country
Mexico
Country Type
NON_EU
Address
2000 Corredor Tijuana-Rosarito Tijuana
Email
service@corza.com
Authorized Representative
SRN
DE-AR-000005767
Country
Germany
Address
2 Allmendweg Jestetten
Email
david.arlt@corza.com
Regulatory Information
Competent Authority
DE/CA39, Regierungsprรคsidium Freiburg Referat 25
Applicable Legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed On The Market
Germany
Market Available
Germany:2021-08-01~None
Device Characteristics
Human Tissues
No
Animal Tissues
No