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Blood Collection Tube - K3 EDTA - India CDSCO Medical Device Registration

Blood Collection Tube - K3 EDTA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000070_9b4956e840ec193827dba8b1a8237e23_6e06b6be34c7164808d8869d17c81b00. This device is marketed under the brand name Vacuum. The license holder is KRIYA Medical Technologies Private Limited, and it is classified as Device Class Class A. The approving authority is Tamil Nadu.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class A
Blood Collection Tube - K3 EDTA
UID: MFG/IVD/2022/000070_9b4956e840ec193827dba8b1a8237e23_6e06b6be34c7164808d8869d17c81b00

Brand Name

Vacuum

Device Class

Class A

Approving Authority

Tamil Nadu

Product Information

A sterile plastic tube, sealed with a stopper, containing a pre-measured amount of vacuum and the anticoagulant tripotassium ethylene diamine tetraacetic acid (Vacuum). It is intended to be used for the collection, and preservation and/or transport, of blood for analysis and/or other investigation [e.g., whole blood haematology such as complete blood count (Vacuum), and quantitative drug assay determinations]. This is a single-use device.

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