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Urea – NED DYE - India CDSCO Medical Device Registration

Urea – NED DYE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000072_c50e606a55bed7eae75ee06e318fa44a_84218acc31ac56dbef83c3ecaad41f26. The license holder is Yucca Diagnostics, and it is classified as Device Class Class B. The approving authority is Pune Division.

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CDSCO Registered
Class Class B
Urea – NED DYE
UID: MFG/IVD/2022/000072_c50e606a55bed7eae75ee06e318fa44a_84218acc31ac56dbef83c3ecaad41f26

License Holder

Yucca Diagnostics

Device Class

Class B

Approving Authority

Pune Division

Product Information

The reagent kit is intended for "in vitro" Quantitative determination of Urea in Serum/Plasma. It is intended for professional in-vitro diagnostic use only

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