B961DP786162910

LEMINECTOMY PUNCHES FERRIS- SMITH-KERRISON 180MM 5MM WITH EJECTOR

Daddy D Pro·Class I·EU EUDAMED·Trade name: LEMINECTOMY PUNCHES FERRIS- SMITH-KERRISON 180MM 5MM WITH EJECTORNo
Device classification
Risk class
Class I
CND nomenclatures code
L091307
Trade name
LEMINECTOMY PUNCHES FERRIS- SMITH-KERRISON 180MM 5MM WITH EJECTOR
Implantable
No
Reusable
Yes
Measuring function
No
Registration information
Primary DI
B961DP786162910
Basic UDI
B-B961DP786162910
Version date
December 12, 2023
Manufacturer last update
April 28, 2023
Active status
No
Manufacturer
Manufacturer name
Daddy D Pro
Country
Pakistan
Country type
NON_EU
Address
High Rise Building, Masjid E Aqsa, Adalat Garh, Ugoki Road Dhattal Sialkot
Email
export@daddydpro.com
Authorized representative
SRN
DE-AR-000008078
Country
Germany
Address
6 Hans Bunte Strasse Heidelberg
Email
info@antex-medi-solution.de
Telephone
+4915678612574
Regulatory information
Competent authority
DE/CA38 - Regierungspräsidium Karlsruhe
Applicable legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed on the market
Portugal
Market available
Germany:None~None, Poland:None~None, Portugal:None~None, Spain:None~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

ORTHOPAEDIC SURGERY RONGEURS, REUSABLE

About this record

Access comprehensive regulatory information for LEMINECTOMY PUNCHES FERRIS- SMITH-KERRISON 180MM 5MM WITH EJECTOR in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI B961DP786162910 and manufactured by Daddy D Pro in Pakistan.

This page provides complete registration details including trade name (LEMINECTOMY PUNCHES FERRIS- SMITH-KERRISON 180MM 5MM WITH EJECTOR), manufacturer information, authorized representative details, competent authority (DE/CA38 - Regierungspräsidium Karlsruhe), 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.