Dia-Body Pouch Insulin Pump Pouch
- Risk class
- Class I
- CND nomenclatures code
- Z12040180
- Trade name
- Kaio-Dia
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 08994228089195
- Basic UDI
- 8994228UP-BPB1A8
- Active status
- No
- Manufacturer name
- CV ANGRREK LIAR
- Country
- Indonesia
- Country type
- NON_EU
- Address
- Jomblang Barat 666, RT 09 RW 03 Semarang
- info@kaio-care.com
- Name
- Kaio-Dia
- SRN
- FR-AR-000037267
- Country
- France
- Address
- 12 RUE BERTRAND LAGRAULET ST NICOLAS
- info@kaio-dia.eu
- Telephone
- +33780919741
- Competent authority
- Agence Nationale de Sécurité du Médicament et des Produits de Santé
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- France
- Human tissues
- No
- Animal tissues
- No
GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - HARDWARE ACCESSORIES
Access comprehensive regulatory information for Dia-Body Pouch Insulin Pump Pouch in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 08994228089195 and manufactured by CV ANGRREK LIAR in Indonesia.
This page provides complete registration details including trade name (Kaio-Dia), manufacturer information, authorized representative details, competent authority (Agence Nationale de Sécurité du Médicament et des Produits de Santé), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.