United Kingdom MHRA device registration 104876

Aorta punch, single-use

United Kingdom flagUnited Kingdom·General Medical Device·Wexler Surgical Inc·Registered Nov 26, 2024
Registration details
Device ID
104876
MHRA Reference Number
104876
Date Registered
Nov 26, 2024
Last Updated
Nov 19, 2024
Device classification
Device Type
General Medical Device
Devices
Aorta punch, single-use
Type
Class I
Manufacturer
Address
11333 Chimney Rock Road Suite 110
Houston, Texas, United States
Created Date
Sep 17, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
7 CAMPION WAY
BINGHAM, NOTTINGHAM, England, United Kingdom
Postcode: NG13 8 TR
Similar products

Devices with a matching generic name or device type registered with MHRA

Other products from Wexler Surgical Inc

Additional devices registered by the same manufacturer

Other products from same authorized representative

Additional devices represented by UKCApartner4U Limited in the UK

Ultrasound imaging system workstationNov 26, 2024
Type: General Medical Device
Manufacturer: MedCom Gesellschaft fur medizinische Bildverarbeitung mbH
Device ID: 112094
Biphasic culture medium IVDNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: HiMedia Laboratories Private Ltd.
Device ID: 145532
Antifungal minimum inhibitory concentration (MIC) IVDNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: HiMedia Laboratories Private Ltd.
Device ID: 132414
Antifungal susceptibility testing disc IVDNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: HiMedia Laboratories Private Ltd.
Device ID: 132417
Antimicrobial activity testing agar culture medium IVDNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: HiMedia Laboratories Private Ltd.
Device ID: 132398
Bacitracin differentiation disc IVDNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: HiMedia Laboratories Private Ltd.
Device ID: 136863
Basic/simple nutrient broth culture medium IVDNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: HiMedia Laboratories Private Ltd.
Device ID: 132400
Blood culture broth kit IVDNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: HiMedia Laboratories Private Ltd.
Device ID: 132439
Buffered isotonic saline reagent IVDNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: HiMedia Laboratories Private Ltd.
Device ID: 132425
Radiation therapy softwareNov 26, 2024
Type: General Medical Device
Manufacturer: MedCom Gesellschaft fur medizinische Bildverarbeitung mbH
Device ID: 112095
About this record

Aorta punch, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 104876. The device is manufactured by Wexler Surgical Inc from United States, classified as General Medical Device. The authorized representative in the UK is UKCApartner4U 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.

Free DatabasePowered by Pure Global AIMHRA RegisteredGeneral Medical Device