Hemostats Forceps
- Risk class
- Class I
- CND nomenclatures code
- L031399
- Trade name
- Hemostats, Kelly Forceps 14cm, Straight
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 89611030824046
- Basic UDI
- 896110308HemostatsRP
- Version date
- December 11, 2022
- Manufacturer last update
- September 10, 2022
- Active status
- No
- Manufacturer name
- Medicure Instruments
- Country
- Pakistan
- Country type
- NON_EU
- Address
- Sardar Pura, Muzaffar Pur, Sialkot, Punjab 51310 Pakistan Sialkot
- info@medicure.pk
- SRN
- DK-AR-000017664
- Country
- Denmark
- Address
- 52 2 th Blokland Albertslund
- info@techstandi.com
- Telephone
- 08000016832
- Competent authority
- Danish Medicines Agency, Pharmacovigilance & Medical Devices
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Denmark
- Market available
- Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Denmark:None~None, Estonia:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece:None~None, Hungary:None~None, Iceland:None~None, Ireland:None~None, Italy:None~None, Latvia:None~None, Liechtenstein:None~None, Lithuania:None~None, Luxembourg:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Portugal:None~None, Romania:None~None, Slovakia:None~None, Slovenia:None~None, Spain:None~None, Sweden:None~None, Turkey:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
GENERAL SURGERY FORCEPS, REUSABLE - OTHER
Access comprehensive regulatory information for Hemostats Forceps 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 89611030824046 and manufactured by Medicure Instruments in Pakistan.
This page provides complete registration details including trade name (Hemostats, Kelly Forceps 14cm, Straight ), manufacturer information, authorized representative details, competent authority (Danish Medicines Agency, Pharmacovigilance & Medical Devices), 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.