Endomyocardial biopsy forceps, single-use
United Kingdom·General Medical Device·H. + H. Maslanka Chirurgische Instrumente GmbH·Registered Nov 26, 2024- Device ID
- 178295
- MHRA Reference Number
- 178295
- Date Registered
- Nov 26, 2024
- Last Updated
- Jun 22, 2024
- Device Type
- General Medical Device
- Devices
- Endomyocardial biopsy forceps, single-use
- Type
- Class III
- Address
- Stockacher Strasse 172 Tuttlingen, Germany
- Created Date
- Sep 1, 2023
- Relationship Type
- UK Responsible Person
- Address
- 2 St Andrews Place Lewes, East Sussex, England, United KingdomPostcode: BN7 1UP
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by MEDAGENT INTERNATIONAL UK LIMITED in the UK
Endomyocardial biopsy forceps, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 178295. The device is manufactured by H. + H. Maslanka Chirurgische Instrumente GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is MEDAGENT INTERNATIONAL UK LIMITED.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.