Tendon sheath regeneration implant - UK MHRA Medical Device Registration

Tendon sheath regeneration implant is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 204880. The device is manufactured by ProSpon spol. s.r.o. from Czechia, classified as General Medical Device. The authorized representative in the UK is Templar Regulatory Consulting 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.

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Tendon sheath regeneration implant

MHRA Device ID: 204880•Ref: 204880

Device Type

General Medical Device

Devices

Tendon sheath regeneration implant

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Jul 26, 2024

Manufacturer Information

Name

ProSpon spol. s.r.o.

Address

Jiřího Voskovce 3206

Kladno, Czechia

Created Date

Aug 24, 2021

Authorized Representative

Name

Templar Regulatory Consulting Limited

Relationship Type

UK Responsible Person

Address

11 Amor Way

Letchworth Garden City, Hertfordshire, England, United Kingdom

Postcode: SG61UG

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Other Products from ProSpon spol. s.r.o. (3)

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Tendon sheath regeneration implant - UK MHRA Medical Device Registration

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