CDSCO UID IMP/MD/2020/000101_5ddf5cb31abff5922734a2f6a4d440bf_4317e1efc1aefd8f875b83d900edcf4d

Safety Hubber Needle

VYGON INDIA PRIVATE LIMITED·Device Class Class B·India CDSCO·Brand: MANIFOLD
Registration details
UID
IMP/MD/2020/000101_5ddf5cb31abff5922734a2f6a4d440bf_4317e1efc1aefd8f875b83d900edcf4d
Device class
Class B
Brand name
MANIFOLD
Approving authority
CDSCO
Product information
POLYPERF® Safe safety Huber needles are indicated for the administration or withdrawal of fluids through implantable ports, POLYPERF Safe is designed to prevent blood-borne pathogen exposures caused by accidentalneedle punctures
Similar products (6)
Other products with the same name or brand
Torque device
Brand: MANIFOLD
VYGON INDIA PRIVATE LIMITED
Class B
Inflation Device
Brand: MANIFOLD
VYGON INDIA PRIVATE LIMITED
Class B
Inflation Device
Brand: MANIFOLD
VYGON INDIA PRIVATE LIMITED
Class B
Inflation Device
Brand: MANIFOLD
VYGON INDIA PRIVATE LIMITED
Class B
Three ports Manifold
Brand: MANIFOLD
VYGON INDIA PRIVATE LIMITED
Class B
Algaflex Line
Brand: MANIFOLD
VYGON INDIA PRIVATE LIMITED
Class B
Other products from VYGON INDIA PRIVATE LIMITED
Products from the same license holder (10 products)
Direct blood pressure monitoring equipments and pulse oximeter
Brand: MostCare Up Monitor
Class C
Seal One Radial Compression Device
Brand: Seal One
Class B
VY-P syringe for Nutrisafe2 enteral connection
Brand: VY-P syringe for Nutrisafe2 enteral connection
Class B
VY-P syringe for Nutrisafe2 enteral connection
Brand: VY-P syringe for Nutrisafe2 enteral connection
Class B
Venous Implantable port
Brand: Polythese POLYBRANCH
Class D
Venous Implantable port
Brand: Polythese POLYBRANCH
Class D
Torque device
Brand: MANIFOLD
Class B
Inflation Device
Brand: MANIFOLD
Class B
Inflation Device
Brand: MANIFOLD
Class B
Inflation Device
Brand: MANIFOLD
Class B
About this record

Safety Hubber Needle is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000101_5ddf5cb31abff5922734a2f6a4d440bf_4317e1efc1aefd8f875b83d900edcf4d. This device is marketed under the brand name MANIFOLD. The license holder is VYGON INDIA PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is CDSCO.

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.