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CDSCO UID IMP/MD/2018/000057_ccbd67fa006fe17ca1cd434186703ae8_293aa62cfde072802ad2eed353c67583

Ureteral Splint Set/Replacement Ureter Splint(PUROFLEX Ureteral Stent Set

Bard India Healthcare Pvt. Ltd.·Device Class Class B·India CDSCO·Brand: via Cystoscope, Tiemann Tip, Percutaneous Application, AIK, Percutaneous Application, Replacement Ureteral Stent via Cystoscope, Replacement Ureteral Stent, Percutaneous Application
Registration details
UID
IMP/MD/2018/000057_ccbd67fa006fe17ca1cd434186703ae8_293aa62cfde072802ad2eed353c67583
Device class
Class B
Brand name
via Cystoscope, Tiemann Tip, Percutaneous Application, AIK, Percutaneous Application, Replacement Ureteral Stent via Cystoscope, Replacement Ureteral Stent, Percutaneous Application
License holder
Bard India Healthcare Pvt. Ltd.
Approving authority
CDSCO
Product information
•Obstruction of the ureter lumen by stones or coagulum •Urine drainage after stone disintegration by ESWL •Strictures or stenoses of the ureters •Compression of the ureters (via Cystoscope, Tiemann Tip, Percutaneous Application, AIK, Percutaneous Application, Replacement Ureteral Stent via Cystoscope, Replacement Ureteral Stent, Percutaneous Application) •Urine drainage after ureteral surgery •Ureter dilatation before ureterorenoscopy •Prevention of oedema and obstruction after endoscopic intervention on the ureters or kidneys
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About this record

Ureteral Splint Set/Replacement Ureter Splint(PUROFLEX Ureteral Stent Set is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000057_ccbd67fa006fe17ca1cd434186703ae8_293aa62cfde072802ad2eed353c67583. This device is marketed under the brand name via Cystoscope, Tiemann Tip, Percutaneous Application, AIK, Percutaneous Application, Replacement Ureteral Stent via Cystoscope, Replacement Ureteral Stent, Percutaneous Application. The license holder is Bard India Healthcare Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

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