Irrigation/Aspiration set for RTUP (Urology) 2 spikes-Pump Segment RF0501T2S

GUDID 03700512921646

Promepla

Surgical irrigation/aspiration tubing set
Primary Device ID03700512921646
NIH Device Record Key0f70f596-3f5b-49f5-8934-e04f6b980ad6
Commercial Distribution StatusIn Commercial Distribution
Brand NameIrrigation/Aspiration set for RTUP (Urology) 2 spikes-Pump Segment
Version Model NumberRF0501T2S
Catalog NumberRF0501T2S
Company DUNS401020409
Company NamePromepla
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+37797984232
Emailcustomer@rocamed.eu

Device Identifiers

Device Issuing AgencyDevice ID
GS103700512901648 [Primary]
GS103700512911647 [Package]
Contains: 03700512901648
Package: Box 1 [10 Units]
In Commercial Distribution
GS103700512921646 [Package]
Contains: 03700512911647
Package: Box 2 [4 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FHFSystem, Evacuator, Fluid

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2019-11-11
Device Publish Date2016-09-14

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03700512987475 - LumaFlex Double J stent, 2 open tips, Ch/Fr4,8/L.26cm, without wire2024-01-15
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