ELAN 4 SPRAY NOZZLE F/2-RG. HANDPIECE L22 - FDA Registration a6ca8920029ef00ae39400e478e6573f
Access comprehensive regulatory information for ELAN 4 SPRAY NOZZLE F/2-RG. HANDPIECE L22 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a6ca8920029ef00ae39400e478e6573f and manufactured by Aesculap AG. The device was registered on November 15, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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FDA Official Data
a6ca8920029ef00ae39400e478e6573f
ELAN 4 SPRAY NOZZLE F/2-RG. HANDPIECE L22
FDA ID: a6ca8920029ef00ae39400e478e6573f
Local name: ELAN 4 SPRAY NOZZLE F/2-RG.HANDPIECE L22
Device Classification
Brand Name
Aesculap
Registration Information
Analysis ID
a6ca8920029ef00ae39400e478e6573f
Registration Date
November 15, 2022
Manufacturer
Name
Aesculap AGAuthorized Representative

