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Regen Lab Cellular Matrix BCT-HA Kit - HSA Registration DE0503602

Access comprehensive regulatory information for Regen Lab Cellular Matrix BCT-HA Kit in the Singapore medical device market through Pure Global AI's free database. This CLASS D medical device is registered under HSA registration number DE0503602 and owned by Regen Lab SA. The device was registered on September 13, 2019.

This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.

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CLASS D
DE0503602
Regen Lab Cellular Matrix BCT-HA Kit
HSA Registration Number: DE0503602
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Product Description

i. Hyaluronic acid (HA) for use as intra-articular injections for symptomatic treatment of articular pain and mobility improvement, or as intra-dermal injections for hydration of dehydrated and wrinkled skin tissues; and ii. Devices for use in the preparation of PRP with HA

Device Classification
Device Class
CLASS D
Medical Speciality Area
Hematology
Registration Information
Registration Number
DE0503602
Registration Date
September 13, 2019
Change Notification Approval Date
June 10, 2024
Retention Due Date
September 12, 2025
Product Owner
Short Name
Regen Lab SA
Address
En Budron B2, 1052- Le Mont, SWITZERLAND
Registrant
Address
111 NORTH BRIDGE ROAD, PENINSULA PLAZA, #21-01, SINGAPORE 179098
Importer
Address
18 SIN MING LANE, MIDVIEW CITY, #06-17, SINGAPORE 573960
Model Information
Model Name(s)
Cellular Matrix BCT-HA Kit
Model Identifier(s)
BCT-HA-3