Peru DIGEMID registration DM17273E
K-MOD HÍGH THICKNESS LNSERTS, K-MOD SKINNY FEMORAL COMPONENTS, K-MOD REV, K-MOD REV ANALLERGIC.
Device classification
- Product Type
- MEDICAL DEVICE
Registration information
- Analysis ID
- DM17273E
- Registration Date
- July 04, 2019
- Expiration Date
- July 04, 2029
- Creation Date
- March 10, 2025
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for K-MOD HÍGH THICKNESS LNSERTS, K-MOD SKINNY FEMORAL COMPONENTS, K-MOD REV, K-MOD REV ANALLERGIC. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DM17273E and manufactured by GRUPPO BIOIMPIANTI S.R.L.. The device was registered on July 04, 2019.
This page provides complete registration details including product type (MEDICAL DEVICE), manufacturer information, authorized representative details, and regulatory compliance data from the official Peru DIGEMID medical device database. Pure Global AI offers free access to Peru's complete medical device registry.
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