Tissue cryostorage straw
United Kingdom·General Medical Device·REPROLIFE Inc.·Registered Nov 26, 2024- Device ID
- 110713
- MHRA Reference Number
- 110713
- Date Registered
- Nov 26, 2024
- Last Updated
- Aug 17, 2024
- Device Type
- General Medical Device
- Devices
- Tissue cryostorage straw
- Type
- Class IIa
- Name
- REPROLIFE Inc.
- Address
- 2-5-3 9F, Shinjuku, Shinjuku-ku Tokyo, Japan
- Created Date
- Nov 3, 2021
- Relationship Type
- UK Responsible Person
- Address
- Beaver House, 23-38 Hythe Bridge Street Oxford, England, United KingdomPostcode: OX1 2EP
Devices with a matching generic name or device type registered with MHRA
Additional devices represented by MT Promedt Consulting Ltd in the UK
Tissue cryostorage straw is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 110713. The device is manufactured by REPROLIFE Inc. from Japan, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting Ltd.
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